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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-(3-Pyridylhydroxymethyl)phenol hydrochloride → 4-(3-Pyridylmethyl)phenol hydrochloride

HRID 1680030
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HRID 1680030 반응식
[ClH:1].[N:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH:8](O)[C:9]2[CH:14]=[CH:13][C:12]([OH:15])=[CH:11][CH:10]=2)[CH:3]=1>[Pd].C(O)(=O)C>[ClH:1].[N:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH2:8][C:9]2[CH:14]=[CH:13][C:12]([OH:15])=[CH:11][CH:10]=2)[CH:3]=1
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참가 물질

4

반응물 1

HCID 132901344-(3-Pyridylhydroxymethyl)phenol hydrochloride

생성물 1

HCID 132901364-(3-Pyridylmethyl)phenol hydrochloride수율 11.5%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 176Acetic Acid용매

실험 절차

Under an atmosphere of hydrogen, a mixture of 1.9 g of the hydroxymethyl compound (prepared as described in Example 8), 1.0 g of 5% palladium on carbon and 12 ml of acetic acid was stirred at room temperature for 24 hours, and filtered. The filtrate was concentrated under reduced pressure. The residue was dissolved in water, neutralized with sodium bicarbonate, extracted with diethyl ether, and the extract was concentrated under reduced pressure. After addition of 6 N hydrochloric acid to the residue, the solution was concentrated under reduced pressure. The residue was purified by recrystallization from ethanol-diethyl ether to give 0.204 g of the title compound having the following physical characteristics:

후처리

  1. filtrationfiltered
  2. concentrationThe filtrate was concentrated under reduced pressure
  3. dissolutionThe residue was dissolved in water
  4. extractionextracted with diethyl ether
  5. concentrationthe extract was concentrated under reduced pressure
  6. additionAfter addition of 6 N hydrochloric acid to the residue
  7. concentrationthe solution was concentrated under reduced pressure
  8. customThe residue was purified by recrystallization from ethanol-diethyl ether

출처 및 근거

ORD 기록
ord-112b889a83fe4d0f988c0bba84374ce2
출처 데이터셋
uspto-grants-1981_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04271170

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