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Thiomorpholine → HCID 86688897, 화합물

HRID 404637
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인쇄 미리보기

반응식

HRID 404637 반응식
Br[CH:2]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:3]([O:5][CH2:6][CH3:7])=[O:4].CCN(C(C)C)C(C)C.[NH:23]1[CH2:28][CH2:27][S:26][CH2:25][CH2:24]1>C(#N)C>[C:8]1([CH:2]([N:23]2[CH2:28][CH2:27][S:26][CH2:25][CH2:24]2)[C:3]([O:5][CH2:6][CH3:7])=[O:4])[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 67164ThiomorpholineHCID 81531DiisopropylethylamineHCID 97780Ethyl bromophenylacetate

생성물 1

HCID 86688897HCID 86688897, 화합물수율 110.9%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

Ethyl 2-bromo-2-phenylacetate (0.22 ml, 1.23 mmol) was dissolved in acetonitrile (4.0 ml). DIPEA (0.26 ml, 1.481 mmol) and thiomorpholine (0.15 ml, 1.41 mmol) were sequentially added and the solution was stirred at room temperature for 1.5 hours. Acetonitrile was evaporated and the residue was purified by flash chromatography (petroleum ether/EtOAc=95/5) to obtain ethyl 2-phenyl-2-thiomorpholinoacetate (362 mg, quantitative yield) as a colorless oil.

후처리

  1. customAcetonitrile was evaporated
  2. customthe residue was purified by flash chromatography (petroleum ether/EtOAc=95/5)

출처 및 근거

ORD 기록
ord-ab62a2473b1041ffae859d6daacb56ae
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08748613B2

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