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Hydrochloric Acid → Methyl 4-amino-2,5-dimethylthiophene-3-carboxylate

HRID 1577429
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HRID 1577429 반응식
O[N:2]=[C:3]1[CH:7]([CH3:8])[S:6][CH:5]([CH3:9])[CH:4]1[C:10]([O:12][CH3:13])=[O:11].Cl>C(OCC)C>[NH2:2][C:3]1[C:4]([C:10]([O:12][CH3:13])=[O:11])=[C:5]([CH3:9])[S:6][C:7]=1[CH3:8]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 86737305HCID 86737305, 화합물

생성물 1

HCID 11019562Methyl 4-amino-2,5-dimethylthiophene-3-carboxylate수율 47.1%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

A cooled solution of 80 g (0.39 mol) of tetrahydro-4-(hydroxyimino)-2,5-dimethyl-3-thiophenecarboxylic acid, methyl ester (Example D) in 1 L of anhydrous diethyl ether is saturated with dry hydrogen chloride over a period of one hour. The solution is stirred and allowed to reach room temperature over fourteen hours. The resulting precipitate is filtered, dissolved in 200 ml of water, neutralized with concentrated ammonium hydroxide and the aqueous solution is extracted with 200 ml of diethyl ether. The diethyl ether solution is washed with 100 ml of water. The diethyl ether layer is separated, dried over anhydrous Na2SO4 and evaporated to give 34 g of 4-amino-2,5-dimethyl-3-thiophenecarboxylic acid, methyl ester; mp 75°-77° C. after recrystallization from hexane.

후처리

  1. waitto reach room temperature over fourteen hours
  2. filtrationThe resulting precipitate is filtered
  3. dissolutiondissolved in 200 ml of water, neutralized with concentrated ammonium hydroxide
  4. extractionthe aqueous solution is extracted with 200 ml of diethyl ether
  5. washThe diethyl ether solution is washed with 100 ml of water
  6. customThe diethyl ether layer is separated
  7. dry with materialdried over anhydrous Na2SO4
  8. customevaporated

출처 및 근거

ORD 기록
ord-a60f77e84e6e4641907b157b925206e8
출처 데이터셋
uspto-grants-1981_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04287340

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