IP Library › Granted Patent US 10,131,603
Granted Patent B2
US 10,131,603 · App. 15/585,720 · Granted Nov 20, 2018

Method for reducing metal of sugar-alcohol compound and sugar-alcohol compound

Inventors: Takayoshi Nakahara (Jyoetsu, JP); Takeru Watanabe (Jyoetsu, JP); Seiichiro Tachibana (Jyoetsu, JP); Tsutomu Ogihara (Jyoetsu, JP)
Assignee: SHIN-ETSU CHEMICAL CO., LTD.
C07C29/92C07C31/26
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Quick Facts
Patent No.
US 10,131,603
App. No.
15/585,720
Granted
Nov 20, 2018
Kind
B2
Abstract

The present invention provides a method for reducing a metal of a sugar-alcohol compound, the method including the steps of (A) protecting a hydroxyl group of a sugar-alcohol compound containing metal impurities with a protecting group, (B) removing the metal impurities from the sugar-alcohol compound having the hydroxyl group protected with the protecting group, and (C) eliminating the protecting group of the sugar-alcohol compound from which the metal has been removed. There can be provided a method for reducing a metal of a sugar-alcohol compound that can provide a sugar-alcohol compound with a suitable quality for the semiconductor apparatus manufacturing process.

Claims (16)

1. A method for reducing a content of metal impurities of a sugar-alcohol compound, the method comprising the steps of:

(A) protecting a hydroxyl group of a sugar-alcohol compound containing metal impurities with a protecting group;

(B) removing the metal impurities from the sugar-alcohol compound having the hydroxyl group protected with the protecting group; and

(C) eliminating the protecting group of the sugar-alcohol compound from which the metal has been removed, wherein

step (C) is performed by a hydrolysis reaction using deionized water.

2. The method according to claim 1 , wherein the sugar-alcohol compound containing metal impurities is selected from the group consisting of erythritol, threitol, arabinitol, xylitol, ribitol, iditol, galactitol, sorbitol, mannitol, volemitol, perseitol, octitol, inositol, and quercitol.

3. The method according to claim 1 , wherein the step (B) includes (B1) liquid-liquid separation and water washing or (B2) distillation.

4. The method according to claim 2 , wherein the step (B) includes (B1) liquid-liquid separation and water washing or (B2) distillation.

5. The method according to claim 1 , wherein the protecting group is acetonide.

6. The method according to claim 2 , wherein the protecting group is acetonide.

7. The method according to claim 3 , wherein the protecting group is acetonide.

8. The method according to claim 4 , wherein the protecting group is acetonide.

9. The method according to claim 1 , wherein the sugar-alcohol compound obtained by the method has a sodium impurity content of 100 ppb or less.

10. The method according to claim 9 , wherein the sodium impurity content is 50 ppb or less.

11. The method according to claim 1 , wherein the deionized water is used in the presence of an acid catalyst.

12. The method according to claim 11 , wherein the acid catalyst is a mineral acid or a carbonic acid.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 3, 2017
From: NAKAHARA, TAKAYOSHI; WATANABE, TAKERU; TACHIBANA, SEIICHIRO; OGIHARA, TSUTOMU
To: SHIN-ETSU CHEMICAL CO., LTD.
Reel/Frame 042227/0576 →
Priority Claims (1)
JP 2016-124209 · Jun 23, 2016 · national
Continuity (1)
Related Publication 20170369407A1 · Dec 28, 2017