2-Bromobenzyl alcohol → 8-[2-(Hydroxymethyl)phenyl]-1,4-dioxaspiro[4.5]decan-8-ol

HRID 1025682

반응식

HRID 1025682 반응식
Br[C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH2:4][OH:5].[Li]CCCC.[CH2:15]1[O:25][C:18]2([CH2:23][CH2:22][C:21](=[O:24])[CH2:20][CH2:19]2)[O:17][CH2:16]1>C1COCC1>[OH:5][CH2:4][C:3]1[CH:6]=[CH:7][CH:8]=[CH:9][C:2]=1[C:21]1([OH:24])[CH2:22][CH2:23][C:18]2([O:25][CH2:15][CH2:16][O:17]2)[CH2:19][CH2:20]1

참가 물질

5

반응 조건

온도
-4 °C

실험 절차

To a solution of 2-bromobenzyl alcohol (3.0 g, 16 mmol) in THF (40 mL) cooled at −78° C. was added a 2.5 M solution of n-BuLi in hexanes (14.1 mL). The mixture was stirred at −4° C. for 1 hour and cooled back to −78° C. To it was added a solution of 1,4-cyclohexanedione mono-ethylene ketal (2.5 g, 16 mmol) in TIE (10 mL) over 15 minutes. Stirring was continued at −78° C. for 30 minutes and at −4° C. for 1 hour. The reaction was quenched by addition of a solution of NH4Cl in water. The resulting solution was extracted with EtOAc three times. The combined extract was washed with brine, dried over MgSO4 and concentrated. Purification on silica gel eluting with 5% MeOH/CH2Cl2 provided the title compound. MS calculated (M+H)+ 265, found 287 (M+Na)+.

후처리

  1. temperaturecooled back to −78° C
  2. stirringStirring
  3. waitwas continued at −78° C. for 30 minutes and at −4° C. for 1 hour
  4. customThe reaction was quenched by addition of a solution of NH4Cl in water
  5. extractionThe resulting solution was extracted with EtOAc three times
  6. extractionThe combined extract
  7. washwas washed with brine
  8. dry with materialdried over MgSO4
  9. concentrationconcentrated
  10. customPurification on silica gel eluting with 5% MeOH/CH2Cl2

출처 및 근거

ORD 기록
ord-a285c5cecc5441239cfa2db866ebbf76
출처 데이터셋
uspto-grants-2014_05
특허 번호
US08729063B2

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