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Acetic Anhydride → N-Formyl-p-methoxyphenylglycine methyl ester

HRID 37462
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HRID 37462 반응식
[CH3:1][O:2][C:3](=[O:21])[CH2:4][N:5]([C:13]1[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[CH:15][CH:14]=1)[C:6](OC(C)(C)C)=[O:7].C(OC(=O)C)(=O)C>C(O)=O>[CH3:1][O:2][C:3](=[O:21])[CH2:4][N:5]([C:13]1[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[CH:15][CH:14]=1)[CH:6]=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 18469309N-Boc-p-methoxyphenylglycine methyl ester

생성물 1

HCID 19935601N-Formyl-p-methoxyphenylglycine methyl ester

시약·촉매·용매 1

HCID 284Formic Acid용매

실험 절차

In 250 ml of formic acid was dissolved 36.9 g of N-Boc-p-methoxyphenylglycine methyl ester, and the mixture was stirred at room temperature for 3 hours and subsequently at 40°-50° C. for 1 hour. After dropwise addition of 24.8 ml (2.1 eq.) of acetic anhydride, the mixture was stirred at room temperature overnight and 40°-50° C. for 2 hours. After the solvent was distilled off, the residue was neutralized with an aqueous solution of sodium hydrogencarbonate, followed by extraction with ethyl acetate. The organic layer was washed with water and a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. The solvent was distilled off. The crystals were collected by filtration with hexane.

후처리

  1. stirringthe mixture was stirred at room temperature overnight and 40°-50° C. for 2 hours
  2. distillationAfter the solvent was distilled off
  3. extractionfollowed by extraction with ethyl acetate
  4. washThe organic layer was washed with water
  5. dry with materiala saturated aqueous solution of sodium chloride and dried over magnesium sulfate
  6. distillationThe solvent was distilled off
  7. filtrationThe crystals were collected by filtration with hexane

출처 및 근거

ORD 기록
ord-c9643de5a4b04cb2a9a78d3775d719f2
출처 데이터셋
uspto-grants-1995_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05420275

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