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Acetic Anhydride → HCID 10546105, 화합물

HRID 1277388
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HRID 1277388 반응식
[NH:1]([C:14]([O:16][CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)=[O:15])[C@H:2]([C:10]([NH:12][NH2:13])=[O:11])[CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[C:24](OC(=O)C)(=[O:26])[CH3:25]>C1COCC1>[NH:1]([C:14]([O:16][CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)=[O:15])[C@H:2]([C:10]([NH:12][NH:13][C:24]([CH3:25])=[O:26])=[O:11])[CH2:3][C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 7120247N-[(Phenylmethoxy)carbonyl]-L-phenylalanine hydrazide

생성물 1

HCID 10546105HCID 10546105, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

In 50 ml of THF is dissolved 2.03 g (6.5 m mols) of Z-Phe-NH-NH2, and under cooling, 1.4 ml of acetic anhydride and 0.9 ml of TEA are added dropwise. The mixture is stirred at room temperature for 2 hours. The crystals are collected by filtration, washed with diethyl ether and recrystallized from AcOEt. 1.9 g (83%); m.p. 205°-206° C.; [α]D23 -16.4° (c=0.5, DMF); Rf1 =0.60.

후처리

  1. temperatureunder cooling
  2. filtrationThe crystals are collected by filtration
  3. washwashed with diethyl ether
  4. customrecrystallized from AcOEt

출처 및 근거

ORD 기록
ord-12ed4d196a754626be2c181784a8e164
출처 데이터셋
uspto-grants-1981_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04277394

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