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Trityl chloride → 4-Trityloxybutan-1-ol

HRID 234213
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HRID 234213 반응식
[CH2:1]([OH:6])[CH2:2][CH2:3][CH2:4][OH:5].[C:7]1([C:13]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)Cl)[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>N1C=CC=CC=1>[C:13]([O:5][CH2:4][CH2:3][CH2:2][CH2:1][OH:6])([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)([C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1)[C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1
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참가 물질

4

반응물 2

HCID 6456Trityl chlorideHCID 80641,4-Butanediol

생성물 1

HCID 3717024-Trityloxybutan-1-ol수율 41.6%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

To a solution of 45 g of butane-1,4-diol in 0.25 of pyridine, cooled to 0° C., were added 139.4 g of triphenylchloromethane and the mixture was stirred at room temperature for 26 h. The precipitate formed was removed by filtration and the filtrate was evaporated in vacuo. The residue was taken up in 0.5 l of ethyl acetate and the solution was washed successively with 200 ml portions of water, 1N hydrochloric acid, water, 5% sodium bicarbonate solution and brine. The organic layer was dried over sodium sulfate and evaporated in vacuo. Crystallization of the residual material from ethyl acetate/hexane afforded 69.0 g of 4-trityloxy-1-butanol as white crystals of m.p. 73°-74° C.

후처리

  1. customThe precipitate formed
  2. customwas removed by filtration
  3. customthe filtrate was evaporated in vacuo
  4. washthe solution was washed successively with 200 ml portions of water, 1N hydrochloric acid, water, 5% sodium bicarbonate solution and brine
  5. dry with materialThe organic layer was dried over sodium sulfate
  6. customevaporated in vacuo
  7. customCrystallization of the residual material from ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-e9af9902f91548aa823d4c01ddcf9eaa
출처 데이터셋
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05594135

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