IP Library Granted Patent US 9,126,963
Granted Patent B2
US 9,126,963 · App. 14/147,894 · Granted Sep 8, 2015

Method for producing tetrahydrofuran

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Quick Facts
Patent No.
US 9,126,963
App. No.
14/147,894
Granted
Sep 8, 2015
Kind
B2
Abstract

The present invention relates to a method for producing tetrahydrofuran comprising: feeding raw material 1,4-butanediol containing gamma butyrolactone to a reaction tank, and performing a dehydration cyclization reaction in the presence of a homogeneous acid catalyst having a pKa of 4 or less and being dissolvable in 1,4-butanediol to produce tetrahydrofuran, wherein a gas containing tetrahydrofuran, gamma butyrolactone and water in the reaction tank is introduced into a heat exchanger and when obtaining a condensate from the outlet of the heat exchanger, the ratio of the concentration of gamma butyrolactone in the condensate based on the concentration of gamma butyrolactone in the raw material 1,4-butanediol is from 20 to 100%.

Claims (10)

1. A method for producing tetrahydrofuran, comprising:

feeding raw material 1,4-butanediol comprising gamma butyrolactone to a reaction tank;

performing a dehydration cyclization reaction to produce tetrahydrofuran in the presence of a homogeneous acid catalyst having a pKa of 4 or less and dissolvable in 1,4-butanediol;

introducing a gas comprising tetrahydrofuran, gamma butyrolactone, and water in the reaction tank into a heat exchanger; and

obtaining a condensate from an outlet of the heat exchanger,

wherein a ratio of a concentration of gamma butyrolactone in the condensate with respect to a concentration of gamma butyrolactone in the raw material 1,4-butanediol is from 20 to 100%.

2. The method according to claim 1 , wherein a temperature of a liquid phase in the reaction tank is from 80 to 250° C.

3. The method according to claim 1 , wherein a concentration of the homogeneous acid catalyst in the reaction tank is from 0.01 to 20.0 wt %.

4. The method according to claim 1 , wherein the homogeneous acid catalyst is mixed with and dissolved in the raw material 1,4-butanediol and then fed to the reaction tank.

5. The method according to claim 1 , wherein a concentration of gamma butyrolactone in the reaction tank is maintained at from 20 ppm by weight to 1 wt %.

Assignments (3)
CHANGE OF NAME Recorded Sep 5, 2017
From: MITSUBISHI RAYON CO., LTD.
To: MITSUBISHI CHEMICAL CORPORATION
Reel/Frame 043750/0834 →
MERGER Recorded Sep 4, 2017
From: MITSUBISHI CHEMICAL CORPORATION
To: MITSUBISHI RAYON CO., LTD.
Reel/Frame 043750/0207 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 5, 2014
From: IZAWA, YUSUKE; UTSUNOMIYA, MASARU; HATTORI, EIJI
To: MITSUBISHI CHEMICAL CORPORATION
Reel/Frame 032145/0050 →