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2-Chlorocyclopentanone → 2-acetoxymethyl-5,6-dihydro-4H-cyclopentathiazole

HRID 1654177
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HRID 1654177 반응식
[C:1]([O:4][CH2:5][C:6]([NH2:8])=[S:7])(=[O:3])[CH3:2].Cl[CH:10]1[CH2:14][CH2:13][CH2:12][C:11]1=O>CN(C)C=O>[C:1]([O:4][CH2:5][C:6]1[S:7][C:10]2[CH2:14][CH2:13][CH2:12][C:11]=2[N:8]=1)(=[O:3])[CH3:2]
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참가 물질

4

반응물 2

HCID 127512-ChlorocyclopentanoneHCID 11018908Carbamothioylmethyl acetate

생성물 1

HCID 677578922-acetoxymethyl-5,6-dihydro-4H-cyclopentathiazole수율 33.8%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
80 °C

실험 절차

A mixture of 2-acetoxythioacetamide (10 g), 2-chlorocyclopentanone (10.6 g) and dimethylformamide (100 ml) was stirred for 24 hours at 80° C. The reaction mixture was cooled and poured into ice-water (500 ml), followed by extraction twice with ethyl acetate (200 ml). The extract was washed twice with water (100 ml), which was dried over magnesium sulfate, then the solvent was distilled off under reduced pressure. The residue was subjected to a silica gel chromatography (2.5×50 cm), eluting with ethyl acetate-hexane (3:7). The object fraction was concentrated to give 2-acetoxymethyl-5,6-dihydro-4H-cyclopentathiazole (5 g) as a yellow oily product.

후처리

  1. temperatureThe reaction mixture was cooled
  2. extractionfollowed by extraction twice with ethyl acetate (200 ml)
  3. washThe extract was washed twice with water (100 ml), which
  4. dry with materialwas dried over magnesium sulfate
  5. distillationthe solvent was distilled off under reduced pressure
  6. washeluting with ethyl acetate-hexane (3:7)
  7. concentrationThe object fraction was concentrated

출처 및 근거

ORD 기록
ord-688df7a317ff428e8eb86212c13c335c
출처 데이터셋
uspto-grants-1995_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05405861

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