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Acetic-formic anhydride → HCID 13536744, 화합물

HRID 464758
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반응식

HRID 464758 반응식
[N:1]([CH2:4][C:5]([C:7]1[CH:8]=[CH:9][C:10]2[O:14][C:13]([CH3:16])([CH3:15])[S:12][C:11]=2[CH:17]=1)=[O:6])=[N+]=[N-].[CH:18]([O-])=[O:19].[Na+].C(OC(=O)C)=O>C(O)=O>[CH:18]([NH:1][CH2:4][C:5]([C:7]1[CH:8]=[CH:9][C:10]2[O:14][C:13]([CH3:16])([CH3:15])[S:12][C:11]=2[CH:17]=1)=[O:6])=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 75269Acetic-formic anhydrideHCID 2723810Sodium FormateHCID 13536743HCID 13536743, 화합물

생성물 1

HCID 13536744HCID 13536744, 화합물수율 59.5%

시약·촉매·용매 1

HCID 284Formic Acid용매

실험 절차

10 g of 5-azidoacetyl-2,2-dimethyl-1,3-benzoxathiole (VIII) was added portionwise to a cooled solution of 20 g stannous chloride and 7 g sodium formate in the mixture of 16 ml of acetic-formic anhydride and 9 ml of formic acid. After 14 hours at room temperature the mixture was quenched with ice and dilute hydrochloric acid and extracted with ethyl acetate. The extract was dried over MgSO4, evaporated, and the residue purified by chromatography through a column of silica gel eluted with ethyl acetate-hexane (1:1) to yield 6 g of 5-formamidoacetyl-2,2-dimethyl-1,3-benzoxathiole (IX) as a yellow oil.

후처리

  1. customAfter 14 hours at room temperature the mixture was quenched with ice and dilute hydrochloric acid
  2. extractionextracted with ethyl acetate
  3. dry with materialThe extract was dried over MgSO4
  4. customevaporated
  5. customthe residue purified by chromatography through a column of silica gel
  6. washeluted with ethyl acetate-hexane (1:1)

출처 및 근거

ORD 기록
ord-3c610817406e44599c350c0c6eeeed72
출처 데이터셋
uspto-grants-1985_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04548951

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