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Methyl Isocyanate → 3-Isopropyl-2-[O-(methylcarbamoyl) oximino]-4-thiazolidinone

HRID 1659140
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인쇄 미리보기

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HRID 1659140 반응식
[CH:1]([N:4]1[C:8](=[O:9])[CH2:7][S:6][C:5]1=[N:10][OH:11])([CH3:3])[CH3:2].[CH3:12][N:13]=[C:14]=[O:15]>CC(C)=O.C(#N)C.C(N(CC)CC)C>[CH:1]([N:4]1[C:8](=[O:9])[CH2:7][S:6][C:5]1=[N:10][O:11][C:14](=[O:15])[NH:13][CH3:12])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 12228Methyl IsocyanateHCID 713968552-(Hydroxyimino)-3-(propan-2-yl)-1,3-thiazolidin-4-one

생성물 1

HCID 867336383-Isopropyl-2-[O-(methylcarbamoyl) oximino]-4-thiazolidinone

시약·촉매·용매 2

HCID 8471Triethylamine촉매HCID 21918305Acetone acetonitrile용매

실험 절차

To a solution of 1.0 g of 3-isopropyl-2-oximino-4-thiazolidinone in 50 ml acetone-acetonitrile solution (1:1) was added 1 ml of methylisocyanate and 5 drops of triethylamine. The reaction mixture was placed in a pressure bottle and left overnight at ambient temperature. After concentrating under vacuo the residual oil was diluted with diethylether. On cooling the product crystallized. Recrystallized from ethyl ether. Weight 1.8 g. m.p. 94°-96°C.

후처리

  1. concentrationAfter concentrating under vacuo the residual oil
  2. additionwas diluted with diethylether
  3. temperatureOn cooling the product
  4. customcrystallized
  5. customRecrystallized from ethyl ether

출처 및 근거

ORD 기록
ord-a617895ddbfa447f9667cda27f19deeb
출처 데이터셋
uspto-grants-1976_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03966953

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