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Triethylamine → HCID 178504143, 화합물

HRID 1982077
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HRID 1982077 반응식
Cl[C:2](OC)=[S:3].N[C:7]1[CH:8]=[C:9]([N:13]2[C:17](=[O:18])[CH2:16][C:15]([CH3:20])([CH3:19])[C:14]2=[O:21])[CH:10]=[CH:11][CH:12]=1.C([N:24]([CH2:27]C)CC)C>CC(C)=O>[CH3:2][SH:3]=[C:27]([C:7]1[CH:8]=[C:9]([N:13]2[C:17](=[O:18])[CH2:16][C:15]([CH3:20])([CH3:19])[C:14]2=[O:21])[CH:10]=[CH:11][CH:12]=1)[NH2:24]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 554404Methyl chloromethanethioateHCID 13189216N-m-AMINOPHENYL-2,2-DIMETHYLSUCCINIMIDE

생성물 1

HCID 178504143HCID 178504143, 화합물

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

Four and one-half g. of methyl chlorothioformate was added dropwise at ambient temperature to a well-stirred mixture of 8.7 g of N-m-aminophenyl-2,2-dimethylsuccinimide, prepared in Example II above, 4.5 g. of triethylamine and 100 ml. of acetone. When the reaction was complete (approximately 30 minutes), the mixture was poured into approximately 500 ml. of water and the product, which crystallized from solution, was collected by filtration and dried. Yield was 9.3 g. of a product having a m.p. of 128°-129° C. The product was identified as the title compound by analysis of infrared spectra.

후처리

  1. customprepared in Example II above, 4.5 g
  2. custom(approximately 30 minutes)
  3. additionthe mixture was poured into approximately 500 ml
  4. customof water and the product, which crystallized from solution
  5. filtrationwas collected by filtration
  6. customdried

출처 및 근거

ORD 기록
ord-4f4a14278ee3483facf29e2000e494e0
출처 데이터셋
uspto-grants-1986_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04595408

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