Nitric Acid → 4-(5-Nitro-thiophen-2-yl)-butyric acid methyl ester

HRID 1178617

반응식

HRID 1178617 반응식
[N+:1]([O-:4])(O)=[O:2].[CH3:5][O:6][C:7](=[O:16])[CH2:8][CH2:9][CH2:10][C:11]1[S:12][CH:13]=[CH:14][CH:15]=1>C(OC(=O)C)(=O)C>[CH3:5][O:6][C:7](=[O:16])[CH2:8][CH2:9][CH2:10][C:11]1[S:12][C:13]([N+:1]([O-:4])=[O:2])=[CH:14][CH:15]=1

참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 1407664-(2-Thienyl)butanoic acid methyl ester

생성물 1

HCID 692334004-(5-Nitro-thiophen-2-yl)-butyric acid methyl ester

시약·촉매·용매 1

HCID 7918Acetic Anhydride용매2회

실험 절차

To 8 mL of acetic anhydride at −20° C. is added 1.2 mL of nitric acid (d=1.5). The mixture is kept at −20° C., and a solution of 4-thiophen-2-yl-butyric acid methyl ester (1.84 g, 10.0 mmol) in 12 mL of acetic anhydride is added dropwise. The reaction mixture is stirred for 10 minutes after completion of addition, and poured into an ice-water mixture. The product is extracted with ethyl acetate and the organic layer is washed with 10 N aqueous sodium hydroxide solution, dried and concentrated. The residue is purified by flash column chromatography eluting with 1:4 ethyl acetate:hexane to provide 1.32 g of 4-(5-nitro-thiophen-2-yl)-butyric acid methyl ester as a yellow oil; 1H NMR (DMSO-d6) δ 1.93 (quintet, J=7 Hz, 2H), 2.41 (t, J=7 Hz, 2H), 2.88 (t, J=7 Hz, 2H), 3.59 (s, 3H), 7.04 (d, J=5 Hz, 1H), 8.01 (d, J=5 Hz, 1H); MS 229.0 (M)+

후처리

  1. customis kept at −20° C.
  2. additionafter completion of addition
  3. extractionThe product is extracted with ethyl acetate
  4. washthe organic layer is washed with 10 N aqueous sodium hydroxide solution
  5. customdried
  6. concentrationconcentrated
  7. customThe residue is purified by flash column chromatography
  8. washeluting with 1:4 ethyl acetate

출처 및 근거

ORD 기록
ord-ce786d9bf66a402ab74423ada59df1fb
출처 데이터셋
uspto-grants-2007_10
특허 번호
US07276519B2

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