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Triethylamine → HCID 18387738, 화합물

HRID 2271016
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HRID 2271016 반응식
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[CH:11]=[CH:10][C:9]([OH:12])=[CH:8][CH:7]=1.C(N(CC)CC)C.[CH3:20][S:21](Cl)(=[O:23])=[O:22]>CC#N>[CH3:20][S:21]([O:12][C:9]1[CH:10]=[CH:11][C:6]([C:2]2[S:1][CH:5]=[CH:4][CH:3]=2)=[CH:7][CH:8]=1)(=[O:23])=[O:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 35641974-Thiophen-2-ylphenol

생성물 1

HCID 18387738HCID 18387738, 화합물수율 63.8%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a mixture of 4-(2-thienyl)phenol (1.76 g) and triethylamine (1.50 g) in MeCN (10 ml) was added dropwise methanesulfonylchloride (1.26 g) with ice-cooling. The mixture was stirred for 1 hour, then for 1 hour at ambient temperature. The resulting mixture was concentrated and diluted with a mixture of AcOEt and H2O to separate solid. The separated solid was recovered and washed with H2O and AcOEt to give 1.62 g of 2-(4-methanesulfonyloxyphenyl)thiophene.

후처리

  1. temperaturecooling
  2. waitfor 1 hour at ambient temperature
  3. concentrationThe resulting mixture was concentrated
  4. additiondiluted with a mixture of AcOEt and H2O
  5. customto separate solid
  6. customThe separated solid was recovered
  7. washwashed with H2O and AcOEt

출처 및 근거

ORD 기록
ord-2843c759c09148aa83e08f37c873688a
출처 데이터셋
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06333324B1

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