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

Carbon tetrabromide → 4-Bromomethylbenzenesulfonamide

HRID 1162193
노트
인쇄 미리보기

반응식

HRID 1162193 반응식
O[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([NH2:12])(=[O:11])=[O:10])=[CH:5][CH:4]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(Br)(Br)(Br)[Br:33]>C(Cl)Cl>[Br:33][CH2:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([NH2:12])(=[O:11])=[O:10])=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11205Carbon tetrabromideHCID 11776TriphenylphosphineHCID 100811624-(Hydroxymethyl)benzenesulfonamide

생성물 1

HCID 131545004-Bromomethylbenzenesulfonamide수율 50%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

4-hydroxymethyl-benzene-sulphonamide (0.105 mg, 0.56 mmoles) was dissolved in DCM (5 mL). Polymer supported triphenylphosphine (294 mg, 2.4 mmoles/g, 1.12 mmoles) was added, and the mixture was stirred with a shaker at room temperature for 10 minutes. CBr4 (557 mg, 1.68 mmoles) was then added, and stirring was continued for 3 hours. The supported reagent was removed by filtration, the solvent was evaporated, and the crude material was purified by flash chromatography (SiO2, petroleum ether/AcOEt 9/1) to yield the title compound as a light-yellow solid (70 mg).

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. additionwas added
  2. stirringstirring
  3. waitwas continued for 3 hours
  4. customThe supported reagent was removed by filtration
  5. customthe solvent was evaporated
  6. customthe crude material was purified by flash chromatography (SiO2, petroleum ether/AcOEt 9/1)

출처 및 근거

ORD 기록
ord-959b2cf596024fef80905e822d391f51
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07820698B2

반응 노트

불러오는 중…