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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Formaldehyde → 6-(Hydroxymethyl)-2-methylpyridin-3-ol

HRID 1606307
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HRID 1606307 반응식
[OH:1][C:2]1[C:3]([CH3:8])=[N:4][CH:5]=[CH:6][CH:7]=1.[OH-:9].[Na+].O.[CH2:12]=O>C(O)(=O)C>[OH:1][C:2]1[C:3]([CH3:8])=[N:4][C:5]([CH2:12][OH:9])=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 712Formaldehyde2회HCID 962WaterHCID 14798Sodium HydroxideHCID 707192-Methylpyridin-3-ol

생성물 1

HCID 123972606-(Hydroxymethyl)-2-methylpyridin-3-ol

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A mixture of 27.2 g. (0.25 mol) of 3-hydroxy-2-methylpyridine, 100 ml. of 10% sodium hydroxide in 75 ml. of water and 22.5 ml. (0.25 mol) of 40% formalin (aqueous methanolic formaldehyde solution) is refluxed for two hours. An additional amount of 40% formalin (22.5 ml.) is added and the reflux is continued for two hours. The mixture is acidified with acetic acid and the resulting precipitate is filtered and washed with acetone. The filtrate is evaporated to dryness and the residue is repeatedly extracted with hot acetone. The extract is dried, treated with charcoal and evaporated to give crude 3-hydroxy-6-hydroxymethyl-2-methylpyridine as a solid.

후처리

  1. additionA mixture of 27.2 g
  2. filtrationthe resulting precipitate is filtered
  3. washwashed with acetone
  4. customThe filtrate is evaporated to dryness
  5. extractionthe residue is repeatedly extracted with hot acetone
  6. customThe extract is dried
  7. additiontreated with charcoal
  8. customevaporated

출처 및 근거

ORD 기록
ord-c2ac2dd992a4428c984cfc99a93c0289
출처 데이터셋
uspto-grants-1976_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03952101

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