홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Iodine → (2-Chloro-4-mercapto-phenoxy)-acetic acid

HRID 1247676
노트
인쇄 미리보기

반응식

HRID 1247676 반응식
P.II.C([O:6][C:7](=[O:21])[CH2:8][O:9][C:10]1[CH:15]=[CH:14][C:13]([S:16](Cl)(=O)=O)=[CH:12][C:11]=1[Cl:20])C.O>C(O)(=O)C>[Cl:20][C:11]1[CH:12]=[C:13]([SH:16])[CH:14]=[CH:15][C:10]=1[O:9][CH2:8][C:7]([OH:21])=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 807IodineHCID 962WaterHCID 24404PhosphineHCID 15145183Ethyl (4-chlorosulfonyl-2-chloro-phenoxy)-acetate

생성물 1

HCID 21908075(2-Chloro-4-mercapto-phenoxy)-acetic acid

시약·촉매·용매 1

HCID 176Acetic Acid용매2회

실험 절차

To a refluxing solution of PH3 (17 g, 500 mmol) and I2 (2.4 g, 9.4 mmol) in glacial acetic acid (100 ml) was added slowly a solution of (4-chlorosulfonyl-2-chloro-phenoxy)-acetic acid ethyl ester (47.5 g, 151 mmol) in glacial acetic acid (1000 ml). The reaction mixture was refluxed for 24 h. Water (20 ml) was added carefully and the mixture was refluxed for further 1 h. After cooling, the reaction mixture was filtered and the filtrate diluted with water (500 ml). The mixture was extracted with dichloromethane (3×100 ml), and the organic phases were washed with water. After drying the dichloromethane phase was evaporated to give crude (2-chloro-4-mercapto-phenoxy)-acetic acid in 17 g yield.

후처리

  1. temperatureThe reaction mixture was refluxed for 24 h
  2. temperaturethe mixture was refluxed for further 1 h
  3. temperatureAfter cooling
  4. filtrationthe reaction mixture was filtered
  5. additionthe filtrate diluted with water (500 ml)
  6. extractionThe mixture was extracted with dichloromethane (3×100 ml)
  7. washthe organic phases were washed with water
  8. dry with materialAfter drying the dichloromethane phase
  9. customwas evaporated

출처 및 근거

ORD 기록
ord-6bb96e95fd9c4f94a20c45c5e7e6c53a
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07129268B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트