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

Hydrochloric Acid → Propanamide, 3,3,3-trifluoro-N-(4-mercaptophenyl)-

HRID 1091826
노트
인쇄 미리보기

반응식

HRID 1091826 반응식
FC(F)(F)CC(=O)[S:5][C:6]1[CH:11]=[CH:10][C:9]([NH:12][C:13](=[O:19])[CH2:14][C:15]([F:18])([F:17])[F:16])=[CH:8][CH:7]=1.CCO.Cl>O>[F:18][C:15]([F:16])([F:17])[CH2:14][C:13]([NH:12][C:9]1[CH:10]=[CH:11][C:6]([SH:5])=[CH:7][CH:8]=1)=[O:19]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 702EthanolHCID 57674935S-4-(3,3,3-trifluoropropanamido)phenyl 3,3,3-trifluoropropanethioate

생성물 1

HCID 57674932Propanamide, 3,3,3-trifluoro-N-(4-mercaptophenyl)-수율 58%

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
50 °C

실험 절차

S-4-(3,3,3-trifluoropropanamido)phenyl 3,3,3-trifluoropropanethioate (44.8 g, 189 mmol) and EtOH (70 mL) were charged to a flask. Concentrated HCl (22.5 mL) was slowly added to keep the temperature below 30° C. The reaction was then heated to 50° C. for 17.5 h. The reaction mixture was reduced to 41 mL by vacuum distillation at 50° C. Cool the reaction to room temperature and H2O (51 mL) was added. The slurry was filtered and the filter cake was washed with H2O (3×35 mL). The solid was dried under vacuum to produce the desired compound (19.9 g, 58%).

후처리

  1. customthe temperature below 30° C
  2. distillationThe reaction mixture was reduced to 41 mL by vacuum distillation at 50° C
  3. temperatureCool
  4. customthe reaction to room temperature
  5. filtrationThe slurry was filtered
  6. washthe filter cake was washed with H2O (3×35 mL)
  7. customThe solid was dried under vacuum

출처 및 근거

ORD 기록
ord-7b196d406c564b1ba5d9844c10d81afc
출처 데이터셋
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08129399B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트