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Hydrochloric Acid → 2-Methyl-3-hydroxy-4-mercaptomethyl-5-vinylpyridine

HRID 461082
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HRID 461082 반응식
[CH3:1][C:2]1[C:7]([OH:8])=[C:6]([CH2:9][S:10]C(=O)C2C=CC=CC=2)[C:5]([CH:19]=[CH2:20])=[CH:4][N:3]=1.[OH-].[Na+].Cl.C(=O)(O)[O-].[Na+]>O1CCCC1>[CH3:1][C:2]1[C:7]([OH:8])=[C:6]([CH2:9][SH:10])[C:5]([CH:19]=[CH2:20])=[CH:4][N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 516892Sodium BicarbonateHCID 202640282-Methyl-3-hydroxy-4-benzoylthiomethyl-5-vinylpyridine

생성물 1

HCID 130669462-Methyl-3-hydroxy-4-mercaptomethyl-5-vinylpyridine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A mixture of 1 g. of 2-methyl-3-hydroxy-4-benzoylthiomethyl-5-vinylpyridine, 10 ml. of tetrahydrofuran, and 10 ml. of 2.5 N aqueous sodium hydroxide was aged at room temperature overnight. The solution was acidified to about pH 6 with hydrochloric acid and then adjusted to pH 7.5 with solid sodium bicarbonate. The mixture was extracted with 3 × 100 ml. of ethyl acetate: isopropanol (9:1 v/v). The extract was dried over magnesium sulfate and concentrated to give 2-methyl-3-hydroxy-4-mercaptomethyl-5-vinylpyridine.

후처리

  1. additionA mixture of 1 g
  2. extractionThe mixture was extracted with 3 × 100 ml
  3. dry with materialThe extract was dried over magnesium sulfate
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-600f1e48f8764fcfb022ff12608b6471
출처 데이터셋
uspto-grants-1977_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04061759

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