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4-Hydroxybenzyl Alcohol → Bromocresol

HRID 25000
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인쇄 미리보기

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HRID 25000 반응식
P(Br)(Br)[Br:2].N1C=CC=CC=1.[OH:11][C:12]1[CH:19]=[CH:18][C:15]([CH2:16]O)=[CH:14][CH:13]=1>C1COCC1>[OH:11][C:12]1[CH:19]=[CH:18][C:15]([CH2:16][Br:2])=[CH:14][CH:13]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1254-Hydroxybenzyl AlcoholHCID 1049PyridineHCID 24614Phosphorus tribromide

생성물 1

HCID 41663Bromocresol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매4회

반응 조건

온도
-20 °C

실험 절차

To a stirred solution of PBr3 (1.38 g, 5.0 mmol) in dry THF (2 ml) at −5° C. was added a solution of dry pyridine (0.201 ml) in dry THF (0.4 ml). A solution of 4-Hydroxybenzyl alcohol (1.89 g, 15.2 mmol) in dry THF (23 ml) was added drop wise to the reaction mixture. The reaction mixture was allowed to stand at room temperature for 18 hours, then diluted with THF and filtered through celite pad. The filtrate was evaporated, the resulting semisolid was redissolved in dry toluene (16 ml). The solution was maintained at −20° C. for 2 hours, and then filtered through celite pad to provide the title compound as a light yellow solution which was used without further purification.

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후처리

  1. filtrationfiltered through celite pad
  2. customThe filtrate was evaporated
  3. dissolutionthe resulting semisolid was redissolved in dry toluene (16 ml)
  4. filtrationfiltered through celite pad

출처 및 근거

ORD 기록
ord-7b0b35eb3ff04b7a9a9875af0715cb58
출처 데이터셋
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06858602B2

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