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Hydroxyamine hydrochloride → 4-Carbomethoxy-3-keto-2-methyltetrahydrothiophene oxime

HRID 2058540
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HRID 2058540 반응식
[C:1]([CH:5]1[CH2:9][S:8][CH:7]([CH3:10])[C:6]1=O)([O:3][CH3:4])=[O:2].Cl.[NH2:13][OH:14]>N1C=CC=CC=1>[C:1]([CH:5]1[CH2:9][S:8][CH:7]([CH3:10])[C:6]1=[N:13][OH:14])([O:3][CH3:4])=[O:2]
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참가 물질

4

반응물 2

HCID 443297Hydroxyamine hydrochlorideHCID 126586981,4-Anhydro-2,5-dideoxy-2-(methoxycarbonyl)-1-thiopent-3-ulose

생성물 1

HCID 737082244-Carbomethoxy-3-keto-2-methyltetrahydrothiophene oxime수율 99%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

A solution of 37.26 g. (0.214 mole) of 4-carbomethoxy-3-keto-2-methyltetrahydrothiophene in 100 ml. anhydrous pyridine was treated with 18.0 g. (0.261 mole) hydroxylamine hydrochloride. The mixture was stirred 24 hours at 25°. The reaction was concentrated and partitioned between 1 N hydrochloric acid/methylene chloride. The aqueous phase was extracted two times with methylene chloride. The combined organic extracts were dried and evaporated to yield 40.1 g (99%) of pure 4-carbomethoxy-3-keto-2-methyltetrahydrothiophene oxime as a colorless oil.

후처리

  1. concentrationThe reaction was concentrated
  2. custompartitioned between 1 N hydrochloric acid/methylene chloride
  3. extractionThe aqueous phase was extracted two times with methylene chloride
  4. customThe combined organic extracts were dried
  5. customevaporated

출처 및 근거

ORD 기록
ord-a653b4fa592b4dd38caa229651a1a4bf
출처 데이터셋
uspto-grants-1982_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04317915

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