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

Benzenesulfonyl chloride → HCID 10924734, 화합물

HRID 1699479
노트
인쇄 미리보기

반응식

HRID 1699479 반응식
[SH:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.[CH2:9](Br)[C:10]#[CH:11].C(N(CC)CC)C.[C:20]1([S:26](Cl)(=[O:28])=[O:27])[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>C(OCC)(=O)C>[C:20]1([S:26]([O:8][C:5]2[CH:6]=[CH:7][C:2]([S:1][CH2:11][C:10]#[CH:9])=[CH:3][CH:4]=2)(=[O:28])=[O:27])[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 7369Benzenesulfonyl chlorideHCID 7842Propargyl bromideHCID 8471Triethylamine2회HCID 2401474-Mercaptophenol

생성물 1

HCID 10924734HCID 10924734, 화합물수율 109.6%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

4-Mercaptophenol (1) (37.85 g, 300 mmol) and propargyl bromide (42.82 g, 360 mmol) were dissolved in ethyl acetate (757 ml). To the solution was added dropwise triethylamine (42.5 g, 420 mmol) over 25 minutes with stirring and under ice-cooling. After stirring for another 1.5 hours at the same temperature, triethylamine (42.5 g, 420 mmol) was added in one portion, and benzenesulfonyl chloride (63.58 g, 360 mmol) was added dropwise over 20 minutes. After keeping 1 hour at the same temperature, the cooling bath was removed and the mixture was stirred for 30 minutes at room temperature and partitioned into two layers by adding ice-water (500 ml) and 2N hydrochloric acid (110 ml). The aqueous layer was extracted with ethyl acetate (200 ml). The combined organic layer was washed with water, dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure to provide 100.04 g of the title compound (2) as oil. Crude yield: 109%.

후처리

  1. temperaturecooling
  2. additionwas added dropwise over 20 minutes
  3. customthe cooling bath was removed
  4. stirringthe mixture was stirred for 30 minutes at room temperature
  5. custompartitioned into two layers
  6. additionby adding ice-water (500 ml) and 2N hydrochloric acid (110 ml)
  7. extractionThe aqueous layer was extracted with ethyl acetate (200 ml)
  8. washThe combined organic layer was washed with water
  9. dry with materialdried over anhydrous magnesium sulfate
  10. distillationthe solvent was distilled off under reduced pressure

출처 및 근거

ORD 기록
ord-188d2f78bb3544e2ae9af02df83b92e8
출처 데이터셋
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06346628B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트