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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 3-[(1-methyl-1H-tetrazol-5-yl)thio]propanoic acid

HRID 2290237
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반응식

HRID 2290237 반응식
C([O:3][C:4](=[O:14])[CH2:5][CH2:6][S:7][C:8]1[N:12]([CH3:13])[N:11]=[N:10][N:9]=1)C.Cl.O>C(O)(=O)C>[CH3:13][N:12]1[C:8]([S:7][CH2:6][CH2:5][C:4]([OH:14])=[O:3])=[N:9][N:10]=[N:11]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 962WaterHCID 15098941Ethyl 3-[(1-methyl-1H-tetrazol-5-yl)sulfanyl]propanoate

생성물 1

HCID 47728753-[(1-methyl-1H-tetrazol-5-yl)thio]propanoic acid

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

5.43 g of 3-(1-methyltetrazol-5-ylthio)-propionic acid ethyl ester are dissolved in 20 ml of acetic acid, 4 ml of conc. HCl and 8 ml of water and the whole is stirred for 3.5 hours at 100°. After concentration of the reaction mixture by evaporation, the residue is partitioned between ethyl acetate and aqueous sodium bicarbonate solution. The aqueous phase is separated off, acidified with 4N HCl and extracted twice with ethyl acetate. After drying and concentration by evaporation the title compound is obtained.

후처리

  1. customAfter concentration of the reaction mixture by evaporation
  2. customthe residue is partitioned between ethyl acetate and aqueous sodium bicarbonate solution
  3. customThe aqueous phase is separated off
  4. extractionextracted twice with ethyl acetate
  5. customAfter drying
  6. concentrationconcentration
  7. customby evaporation the title compound
  8. customis obtained

출처 및 근거

ORD 기록
ord-0f2625481ec04d85a6e0f636a07339d5
출처 데이터셋
uspto-grants-1986_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04616007

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