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Diethyl Ether → Dimethyl 4-aminothiophene-2,3-dicarboxylate Hydrochloride

HRID 231642
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HRID 231642 반응식
O=[C:2]1[CH:6]([C:7]([O:9][CH3:10])=[O:8])[CH:5]([C:11]([O:13][CH3:14])=[O:12])[S:4][CH2:3]1.[ClH:15].[NH2:16]O.CCOCC>C(#N)CC>[ClH:15].[NH2:16][C:2]1[C:6]([C:7]([O:9][CH3:10])=[O:8])=[C:5]([C:11]([O:13][CH3:14])=[O:12])[S:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 443297Hydroxyamine hydrochlorideHCID 2777656Methyl 2,5-anhydro-3-deoxy-3-(methoxycarbonyl)-2-thiopent-4-ulosonate

생성물 1

HCID 2808333Dimethyl 4-aminothiophene-2,3-dicarboxylate Hydrochloride

시약·촉매·용매 1

HCID 7854Propionitrile용매

실험 절차

3-Oxo-4,5-bismethoxycarbonyltetrahydrothiophene (2.65 g) was dissolved in propionitrile (5 ml) and hydroxylamine hydrochloride (1 g) was added. The mixture was heated under reflux on the steam bath for 11/2 hours by which time it was almost solid. Ether was added to the cooled mixture and the title compound was filtered off. Yield 2.37 g (77.5%) M.P.166°-169° dec. 3-Amino-4,5-bismethoxycarbonylthiophene was liberated from the title compound by treatment with aqueous ammonia followed by bulk distillation (220° C., 0.1 mm Hg) and exhibited 'H n.m.r. δ (CDCl3) 6.40 (1H,s), 4.40 (2H, brs), 3.90, 3.94 (2×3H,s).

후처리

  1. temperatureThe mixture was heated
  2. temperatureunder reflux on the steam bath for 11/2 hours by which time it
  3. filtrationthe title compound was filtered off
  4. distillationfollowed by bulk distillation (220° C., 0.1 mm Hg)

출처 및 근거

ORD 기록
ord-6b33ab1601fc441f8dc76a3f6c14efe7
출처 데이터셋
uspto-grants-1989_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04847386

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