CN107540544A - A kind of chloride process of thiazole carboxamides production technology - Google Patents
A kind of chloride process of thiazole carboxamides production technology Download PDFInfo
- Publication number
- CN107540544A CN107540544A CN201610470315.1A CN201610470315A CN107540544A CN 107540544 A CN107540544 A CN 107540544A CN 201610470315 A CN201610470315 A CN 201610470315A CN 107540544 A CN107540544 A CN 107540544A
- Authority
- CN
- China
- Prior art keywords
- chlorine
- solvent
- chlorination
- caused
- recovery
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Landscapes
- Treating Waste Gases (AREA)
Abstract
The invention belongs to chemical products production field, especially thiazole carboxamides production field.Thiazole carboxamides are a kind of important chemical products.Process units is batch production flow, mainly including processes such as bromination, recrystallization, chlorination, cyclization, ammonifications.
Description
Technical field
The invention belongs to chemical products production field, especially thiazole carboxamides production field.
Background technology
Thiazole carboxamides are a kind of important chemical products.Process units is batch production flow, mainly including bromination,
The processes such as recrystallization, chlorination, cyclization, ammonification.
The content of the invention
Production procedure is as follows:
Chlorination reaction
Trifluoroacetic ethyl acetoacetate at low temperature, 2- chlorine trifluoroacetyl acetic acid is obtained in solvent is to two benzotrifluorides by chlorine
Ethyl ester.Chlorination reaction temperature is 0 degree Celsius, and the reaction time is 6 h.The molar ratio of trifluoroacetic ethyl acetoacetate and chlorine
For 1:1.015.The 2- chlorine trifluoroacetic ethyl acetoacetates obtained after solvent are distilled off.Caused hydrogen chloride gas in chlorination process
After 2 grades of falling film absorptions, caused hydrochloric acid is sold as byproduct, again through chlorine recovery device recovery set after falling film absorption
With chlorine almost all in the case where not leaking reclaims.Caused hydrogen chloride gas is after acid gas absorption plant absorbs
Discharge.
Under abnormal condition, chlorine recovery device is stopped, hydrogen chloride(Containing chlorine)Enter acidity again after alkali liquor absorption
Gas concentration unit.In solvent recovery process, it is 110 DEG C to control vapo(u)rizing temperature, distillation time 6h.Two benzotrifluorides are distilled
The emptying of tower and receiving tank, after the cold well cooling buffering of two-stage, there is a small amount of solvent to two benzotrifluorides(G3-5)It is laggard through collecting
Uncontrollable discharge tail gas absorbing system.Solvent recovering rate is 99%.
Reaction equation:
Chlorination
。
Claims (2)
1. the present invention relates to material composition and proportioning.
2. the present invention relates to production procedure:Chlorination reaction, trifluoroacetic ethyl acetoacetate at low temperature, in solvent to two benzotrifluorides
In 2- chlorine trifluoroacetic ethyl acetoacetates are obtained by chlorine;Chlorination reaction temperature is 0 degree Celsius, and the reaction time is 6 h;Trifluoro
The molar ratio of ethyl acetoacetate and chlorine is 1:1.015;The 2- chlorine trifluoroacetyl acetic acid obtained after solvent is distilled off
Ethyl ester;Caused hydrogen chloride gas after 2 grades of falling film absorptions, as byproduct sell by caused hydrochloric acid in chlorination process, drop
Again through chlorine recovery device recovery after film absorption, chlorine almost all in the case where not leaking reclaims;Caused chlorination
Hydrogen discharges after acid gas absorption plant absorbs;Under abnormal condition, chlorine recovery device is stopped, hydrogen chloride
(Containing chlorine)Enter sour gas retracting device again after alkali liquor absorption;In solvent recovery process, it is 110 DEG C to control vapo(u)rizing temperature,
Distillation time is 6h;Emptying to two benzotrifluoride destilling towers and receiving tank, after the cold well cooling buffering of two-stage, there is a small amount of solvent
To two benzotrifluorides(G3-5)Through collecting laggard uncontrollable discharge tail gas absorbing system.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610470315.1A CN107540544A (en) | 2016-06-27 | 2016-06-27 | A kind of chloride process of thiazole carboxamides production technology |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610470315.1A CN107540544A (en) | 2016-06-27 | 2016-06-27 | A kind of chloride process of thiazole carboxamides production technology |
Publications (1)
Publication Number | Publication Date |
---|---|
CN107540544A true CN107540544A (en) | 2018-01-05 |
Family
ID=60960129
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610470315.1A Pending CN107540544A (en) | 2016-06-27 | 2016-06-27 | A kind of chloride process of thiazole carboxamides production technology |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN107540544A (en) |
-
2016
- 2016-06-27 CN CN201610470315.1A patent/CN107540544A/en active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2636662A1 (en) | Process for producing trans-1,3,3,3-tetrafluoropropene | |
JP5850937B2 (en) | Salt water purification method | |
CN105377751A (en) | Method for purifying hydrogen chloride | |
TWI740458B (en) | Abstract of description nitrogen oxide absorption slurry and its preparation and use method thereof | |
WO2013161692A1 (en) | Method for parallel production of trans-1,3,3,3-tetrafluoropropene and 1,1,1,3,3-pentafluoropropane | |
US20130161201A1 (en) | Electrolysis Process | |
US10626015B2 (en) | Process for preparation of hydrobromic acid | |
CN103864615B (en) | A kind of method that continuous on-catalytic method prepares Trifluoroacetic Acid Ethyl Ester | |
CN108276315A (en) | A kind of purification process of trifluoromethanesulfonic acid | |
BRPI0619559A2 (en) | process for chlorine production | |
WO2019114739A1 (en) | Production process for chlorinated paraffin | |
CN106608858A (en) | Production technology of 4-methyl-5-beta-hydroxyethyl thiazole | |
CN107540544A (en) | A kind of chloride process of thiazole carboxamides production technology | |
CN107311838A (en) | A kind of method of new synthesis Cyclopropyl Bromide | |
CN101863803A (en) | Purification method of byproduct hydrochloric acid | |
CN105152914A (en) | Production technology of trichloroacetyl chloride | |
CN105753677A (en) | Method for recovering acetone and diethylamine from mother liquor obtained after propacetamol hydrochloride ammonification | |
CN107973692A (en) | A kind of preparation method of brominated alkanes | |
CN111116306B (en) | Preparation method of hexafluorobenzene | |
CN105523902A (en) | Preparation method of 1-(2-chloroethoxy)propane | |
CN107540578A (en) | A kind of adjacent trifluoromethoxy benzenesulfonyl isocyanate production technology | |
CN105899482B (en) | The manufacturing method of hexachloroacetone | |
CN106431899B (en) | A method of preparing left-handed menthylformic acid | |
CN107540573A (en) | It is a kind of to trifluoromethoxy isocyanates production process | |
CN113511954B (en) | Continuous flow preparation method of 1,2, 3-trichloropropane |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
WD01 | Invention patent application deemed withdrawn after publication | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20180105 |