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Sodium Hydroxide → 4-[(1-Methyl-1H-tetrazol-5-yl)sulfanyl]butanoic acid

HRID 2290232
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HRID 2290232 반응식
C([O:3][C:4](=[O:15])[CH2:5][CH2:6][CH2:7][S:8][C:9]1[N:13]([CH3:14])[N:12]=[N:11][N:10]=1)C.[OH-].[Na+]>C1COCC1>[CH3:14][N:13]1[C:9]([S:8][CH2:7][CH2:6][CH2:5][C:4]([OH:15])=[O:3])=[N:10][N:11]=[N:12]1
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 21295546HCID 21295546, 화합물

생성물 1

HCID 130916224-[(1-Methyl-1H-tetrazol-5-yl)sulfanyl]butanoic acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

2.93 g of 4-(1-methyltetrazol-5-ylthio)-butyric acid ethyl ester are dissolved in 50 ml of THF, 15 ml of 1N NaOH are added and the whole is stirred for 3 hours at room temperature. Most of the THF is then concentrated by evaporation under reduced pressure in a rotary evaporator and the residue is washed with ethyl acetate. The aqueous solution is adjusted to pH 3 with 4N HCl and extracted three times with ethyl acetate. After drying over sodium sulphate and concentration by evaporation under reduced pressure, the pure title compound is obtained.

후처리

  1. concentrationMost of the THF is then concentrated by evaporation under reduced pressure in a rotary evaporator
  2. washthe residue is washed with ethyl acetate
  3. extractionextracted three times with ethyl acetate
  4. dry with materialAfter drying over sodium sulphate and concentration by evaporation under reduced pressure

출처 및 근거

ORD 기록
ord-8c68a04d750d416e8995293d97712081
출처 데이터셋
uspto-grants-1986_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04616007

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