JPH02255649A - 4’―クロロ―2’―トリフルオロメチルプロポキシアセトアニリドの製造法 - Google Patents
4’―クロロ―2’―トリフルオロメチルプロポキシアセトアニリドの製造法Info
- Publication number
- JPH02255649A JPH02255649A JP1076468A JP7646889A JPH02255649A JP H02255649 A JPH02255649 A JP H02255649A JP 1076468 A JP1076468 A JP 1076468A JP 7646889 A JP7646889 A JP 7646889A JP H02255649 A JPH02255649 A JP H02255649A
- Authority
- JP
- Japan
- Prior art keywords
- phosphorus
- formula
- chloro
- phosphorus oxychloride
- phosphorus trichloride
- 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.)
- Granted
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 7
- PRFIIMLQPHQGOC-UHFFFAOYSA-N n-[4-chloro-2-(trifluoromethyl)phenyl]-2-propoxyacetamide Chemical compound CCCOCC(=O)NC1=CC=C(Cl)C=C1C(F)(F)F PRFIIMLQPHQGOC-UHFFFAOYSA-N 0.000 title claims 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 claims abstract description 18
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 claims abstract description 10
- 230000005494 condensation Effects 0.000 claims abstract 3
- 238000009833 condensation Methods 0.000 claims abstract 3
- SGUYGLMQEOSQTH-UHFFFAOYSA-N 2-propoxyacetic acid Chemical compound CCCOCC(O)=O SGUYGLMQEOSQTH-UHFFFAOYSA-N 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract description 18
- 238000006243 chemical reaction Methods 0.000 abstract description 10
- 239000003795 chemical substances by application Substances 0.000 abstract description 5
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract description 5
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 abstract description 4
- 229910000040 hydrogen fluoride Inorganic materials 0.000 abstract description 4
- 239000003960 organic solvent Substances 0.000 abstract description 3
- 150000001875 compounds Chemical class 0.000 abstract 4
- RVUYACAXXOCJAH-UHFFFAOYSA-N propyl ethaneperoxoate Chemical compound CCCOOC(C)=O RVUYACAXXOCJAH-UHFFFAOYSA-N 0.000 abstract 3
- CVINWVPRKDIGLL-UHFFFAOYSA-N 4-chloro-2-(trifluoromethyl)aniline Chemical compound NC1=CC=C(Cl)C=C1C(F)(F)F CVINWVPRKDIGLL-UHFFFAOYSA-N 0.000 abstract 1
- 239000003905 agrochemical Substances 0.000 abstract 1
- 230000003301 hydrolyzing effect Effects 0.000 abstract 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 150000003931 anilides Chemical class 0.000 description 8
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- -1 benzene-toluene Chemical compound 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000002912 waste gas Substances 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 150000001448 anilines Chemical class 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- DALDUXIBIKGWTK-UHFFFAOYSA-N benzene;toluene Chemical compound C1=CC=CC=C1.CC1=CC=CC=C1 DALDUXIBIKGWTK-UHFFFAOYSA-N 0.000 description 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- RCJVRSBWZCNNQT-UHFFFAOYSA-N dichloridooxygen Chemical compound ClOCl RCJVRSBWZCNNQT-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1076468A JPH02255649A (ja) | 1989-03-30 | 1989-03-30 | 4’―クロロ―2’―トリフルオロメチルプロポキシアセトアニリドの製造法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1076468A JPH02255649A (ja) | 1989-03-30 | 1989-03-30 | 4’―クロロ―2’―トリフルオロメチルプロポキシアセトアニリドの製造法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02255649A true JPH02255649A (ja) | 1990-10-16 |
JPH0588703B2 JPH0588703B2 (enrdf_load_stackoverflow) | 1993-12-24 |
Family
ID=13606002
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1076468A Granted JPH02255649A (ja) | 1989-03-30 | 1989-03-30 | 4’―クロロ―2’―トリフルオロメチルプロポキシアセトアニリドの製造法 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02255649A (enrdf_load_stackoverflow) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110105289B (zh) * | 2019-04-11 | 2022-04-26 | 江苏禾本生化有限公司 | 一种氟菌唑原药及其制备方法 |
-
1989
- 1989-03-30 JP JP1076468A patent/JPH02255649A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPH0588703B2 (enrdf_load_stackoverflow) | 1993-12-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN111732520B (zh) | 一种3-甲基-2-氨基苯甲酸的制备方法 | |
CN108503531B (zh) | 一种3,3-二甲基-2-氧代丁酸的制备方法 | |
CN107641106A (zh) | 法匹拉韦中间体以及法匹拉韦的合成方法 | |
CN102964207A (zh) | 一种2-溴-3,3,3-三氟丙烯的制备方法 | |
JPH02255649A (ja) | 4’―クロロ―2’―トリフルオロメチルプロポキシアセトアニリドの製造法 | |
CN112023957A (zh) | 一种基于b-p-o基团催化剂及其制备色酚的方法 | |
CN111620876A (zh) | 瑞德西韦关键中间体的合成方法 | |
CN108947868A (zh) | 一种2,4-二氟苯腈的制备工艺 | |
JPH02255650A (ja) | 4′―クロロ―2′―トリフルオロメチルプロポキシアセトアニリドの製造方法 | |
JP3729884B2 (ja) | フルオロフェノール類の製造方法 | |
CN117550981B (zh) | 一种2-氨基-5-氟苯乙酮的制备方法 | |
CN116023295B (zh) | 一种1,1-二卤甲醛肟的合成方法 | |
JPH02258753A (ja) | 4’―クロロ―2’―トリフルオロメチルプロポキシアセトアニリドの製造方法 | |
JP4376387B2 (ja) | シアノベンジル化合物の製造方法 | |
JPS63162641A (ja) | ペンタエリスリト−ルアリルエ−テルの製造法 | |
JPH0469132B2 (enrdf_load_stackoverflow) | ||
JPS6212741A (ja) | 2−ペルフルオロアルキルアクリル酸の製造方法 | |
JPS61186373A (ja) | チオシアネートメチルチオベンゾチアゾール類の製造方法 | |
JPH02193946A (ja) | メチルジクロロフルオロアセテートの製造法 | |
CN1733665A (zh) | 由氟苯制造对溴氟苯的方法 | |
JP5209201B2 (ja) | 分子内に不飽和基を有する高純度有機酸クロライドの製造方法 | |
JPS60218349A (ja) | ベンズアルデヒド類の製造法 | |
WO2022000160A1 (zh) | 一种烷烃选择性催化氧化反应的方法 | |
JPS6219420B2 (enrdf_load_stackoverflow) | ||
CN111592465A (zh) | 一种制备2-氨基-4-氨甲基苯甲酸甲酯及其盐酸盐的方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20081224 Year of fee payment: 15 |
|
LAPS | Cancellation because of no payment of annual fees |