IP Library Granted Patent US 9,637,466
Granted Patent B2
US 9,637,466 · App. 14/904,226 · Granted May 2, 2017

Liquid crystal compound having 2, 6-difluorophenyl ether structure and liquid crystal composition thereof

Inventors: Kenta Tojo (Kitaadachi-gun, JP); Tetsuo Kusumoto (Kitaadachi-gun, JP)
Assignee: DIC CORPORATION
C07D319/06C09K19/0403C09K19/3402C09K2019/3422
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,637,466
App. No.
14/904,226
Granted
May 2, 2017
Kind
B2
Abstract

The present invention relates to a compound having 2,6-difluorophenyl ether structure and useful as an organic electronic material and a medicine/agrochemical, particularly a material for liquid crystal display devices, and also relates to an effective method for producing the same. The present invention provides a compound represented by general formula (1) and also provides a liquid crystal composition containing the compound and a liquid crystal display device using the liquid crystal composition. A liquid crystal composition exhibiting low viscosity and a liquid crystal phase within a wide temperature range can be produced by using the compound represented by the general formula (1) as a component of the liquid crystal composition. Thus, the compound is very useful as a constituent component of a liquid crystal composition for a liquid crystal display device required to have, fast response.

Claims (33)

1. A compound represented by general formula (1),

wherein in the formula (1), R represents an alkyl group having 1 to 15 carbon atoms or an alkenyl group having 2 to 15 carbon atoms, one —CH 2 — or two or more unadjacent —CH 2 — present in the group is/are optionally substituted by —O—, —S—, —COO—, —OCO—, or —CO—, and a hydrogen atom present in the group is optionally substituted by a fluorine atom,

A 1 , A 2 , A 3 , and A 4 each independently represent a group selected from the group consisting of

(a) a 1,4-cyclohexylene group wherein one —CH 2 — or two or more unadjacent —CH 2 — present in the group is/are optionally substituted by —O— or —S—;

(b) a 1,4-phenylene group wherein one —CH═ or two or more unadjacent —CH═ present in the group is/are optionally substituted by —N═, and a hydrogen atom present in the group is optionally substituted by a fluorine atom; and

(c) a naphthalene-2,6-diyl group wherein a hydrogen atom present in the group is/are optionally substituted by a fluorine atom,

Z 1 , Z 2 , Z 3 , and Z 4 each independently represent —CH 2 O—, —OCH 2 —, —CF 2 O—, —OCF 2 —, —CH 2 CH 2 —, —CF 2 CF 2 —, —CH═CH—, —CF═CF—, —C≡C—, or a single bond,

A 5 represents

wherein in the formulae, W represents a fluorine atom, a chlorine atom, a cyano group, —CF 3 , —OCH 2 F, —OCHF 2 , or —OCF 3 , and Y 1 , Y 2 , Y 3 , Y 4 , and Y 5 each independently represent a fluorine atom, a chlorine atom, or a hydrogen atom,

m, n, p, and r each independently represent 0 or 1, and m+n+p+r is 0, 1, 2, or 3.

2. The compound according to claim 1 , wherein in the general formula (1), A 1 , A 2 , A 3 , and A 4 each independently represent a group selected from

3. The compound according to claim 1 , wherein in the general formula (1), Z 1 , Z 2 , Z 3 , and Z 4 each independently represent —OCH 2 —, —CF 2 O—, —CH 2 CH 2 —, —C≡C—, or a single bond.

4. The compound according to claim 1 , wherein in the general formula (1), W represents a fluorine atom, a cyano group, or —OCF 3 .

5. The compound according to claim 1 , wherein in the general formula (1), A 5 represents

6. The compound according to claim 1 , wherein in the general formula (1), A 5 represents

7. The compound according to claim 1 , wherein the compound represented by the general formula (1) is a compound represented by general formula (1a) to general formula (1j)

wherein in the formulae, R, W, Y 1 , Y 2 , Y 3 , Y 4 , and Y 5 each independently represent the same meaning as R, W, Y 2 , Y 3 , Y 4 , and Y 5 in the general formula (1), Y 10 , Y 11 , Y 12 ,Y 13 , Y 14 and Y 15 each independently represent a fluorine atom, or a hydrogen atom, and A 7 ,A 8 , and A 9 each independently represent

(a) 1,4-cyclohexylene group wherein one —CH 2 — or two or more unadjacent —CH 2 — present in the group is/are optionally substituted by —O— or —S—; or

(b) 1,4-phenylene group wherein one —CH═ or two or more unadjacent —CH═ present in the group is/are optionally substituted by —N═, and a hydrogen atom present in the group is optionally substituted by a fluorine atom.

8. A liquid crystal composition comprising one or two or more compounds according to claim 1 .

9. A liquid crystal display device using the liquid crystal composition according to claim 8 .

10. A production method comprising reacting a compound represented by general formula (2)

wherein in the formula, X 1 represents a chlorine atom, a bromine atom, a methanesulfonyloxy group, a p-toluenesulfonyloxy group, or a hydroxyl group, and A 3 , A 4 , A 5 , Z 3 , Z 4 , p, and r each independently represent the same meaning as A 3 , A 4 , A 5 , Z 3 , Z 4 , p, and r in the general formula (1) with a compound represented by general formula (3)

wherein in the formula, R, A 1 , A 2 , Z 1 , Z 2 , m, and n each independently represent the same meaning as R, A 1 , A 2 , Z 1 , Z 2 , m, and n in the general formula (1), thereby producing a compound represented by general formula (1),

wherein in the formula, R represents an alkyl group having 1 to 15 carbon atoms or an alkenyl group having 2 to 15 carbon atoms, one —CH 2 — or two or more unadjacent —CH 2 — present in the group is/are optionally substituted by —O—, —S—, —COO—, —OCO—, or —CO—, and a hydrogen atom present in the group is optionally substituted by a fluorine atom,

A 1 , A 2 , A 3 , and A 4 each independently represent a group selected from the group consisting of

(a) a 1,4-cyclohexylene group wherein one —CH 2 — or two or more unadjacent —CH 2 — present in the group is/are optionally substituted by —O— or —S—;

(b) a 1,4-phenylene group wherein one —CH═ or two or more unadjacent —CH═ present in the group is/are optionally substituted by —N═, and a hydrogen atom present in the group is optionally substituted by a fluorine atom; and

(c) a naphthalene-2,6-diyl group wherein a hydrogen atom present in the group is optionally substituted by a fluorine atom,

Z 1 , Z 2 , Z 3 , and Z 4 each independently represent —CH 2 O—, —OCH 2 —, —CF 2 O—, —OCF 2 —, —CH 2 CH 2 —, —CF 2 CF 2 —, —CH═CH—, —CF═CF—, —C≡C—, or a single bond,

A 5 represents

wherein in the formulae, W represents a fluorine atom, a chlorine atom, a cyano group, —CF 3 , —OCH 2 F, —OCHF 2 , or —OCF 3 , and Y 1 , Y 2 , Y 3 , Y 4 , and Y 5 each independently represent a fluorine atom, a chlorine atom, or a hydrogen atom, and

m, n, p, and r each independently represent 0 or 1, and m+n+p+r is 0, 1, 2, or 3.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 24, 2024
From: DIC CORPORATION
To: SHIJIAZHUANG CHENGZHI YONGHUA DISPLAY MATERIAL CO., LTD.
Reel/Frame 067528/0688 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 11, 2016
From: TOJO, KENTA; KUSUMOTO, TETSUO
To: DIC CORPORATION
Reel/Frame 037453/0556 →
Priority Claims (1)
JP 2013-154499 · Jul 25, 2013 · national
Continuity (1)
Related Publication 20160152589A1 · Jun 2, 2016