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Ethyl Acetate → N-(2,2,2-Trichloroethoxycarbonyloxy)succinimide

HRID 894103
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HRID 894103 반응식
[OH:1][N:2]1[C:6](=[O:7])[CH2:5][CH2:4][C:3]1=[O:8].C(OCC)(=O)C.[Cl:15][C:16]([Cl:23])([Cl:22])[CH2:17][O:18][C:19](Cl)=[O:20]>N1C=CC=CC=1>[Cl:15][C:16]([Cl:23])([Cl:22])[CH2:17][O:18][C:19]([O:1][N:2]1[C:6](=[O:7])[CH2:5][CH2:4][C:3]1=[O:8])=[O:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8857Ethyl AcetateHCID 80170N-HydroxysuccinimideHCID 870632,2,2-Trichloroethyl chloroformate

생성물 1

HCID 4192178N-(2,2,2-Trichloroethoxycarbonyloxy)succinimide

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

Dissolve 5.75 gm. of N-hydroxysuccinimide in 200 ml. ethyl acetate and 4 gm. of pyridine; cool the resultant solution to 0° C. To this solution, add 10.6 gm. 2,2,2-trichloroethylchloroformate dropwise over a period of 1.5 hours. Filter the resultant mixture and evaporate the filtrate to dryness. Wash the thereby formed needles with hexane to obtain N-(2,2,2-trichloroethoxycarbonyloxy) succinimide, m.p. 98°-101° C.; ν max. (CHCl3) 1825, 1790, 1750, 1185, 826 cm.-1, δ (CDCl3) 2.85 (4H, s, --CO(CH2)2CO--) and 4.90 ppm (2H, s, --COOCH2CCl3).

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후처리

  1. dissolutionDissolve 5.75 gm
  2. additionTo this solution, add 10.6 gm
  3. filtrationFilter the resultant mixture
  4. customevaporate the filtrate to dryness
  5. washWash the
  6. customthereby formed needles with hexane

출처 및 근거

ORD 기록
ord-990af25831704a208e34b777c0c39f2e
출처 데이터셋
uspto-grants-1981_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04282350

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