Imidazole → (2R)-1-{[Tri(propan-2-yl)silyl]oxy}propan-2-ol

HRID 20590

반응식

HRID 20590 반응식
[CH:1]([Si:4](Cl)([CH:8]([CH3:10])[CH3:9])[CH:5]([CH3:7])[CH3:6])([CH3:3])[CH3:2].[CH2:12]([OH:16])[C@H:13]([OH:15])[CH3:14].N1C=CN=C1>CN(C=O)C>[CH:1]([Si:4]([CH:8]([CH3:10])[CH3:9])([CH:5]([CH3:7])[CH3:6])[O:16][CH2:12][C@H:13]([OH:15])[CH3:14])([CH3:3])[CH3:2]

참가 물질

5

반응물 3

HCID 795ImidazoleHCID 139400Triisopropylsilyl chlorideHCID 259994R-(-)-1,2-Propanediol

생성물 1

HCID 57504697(2R)-1-{[Tri(propan-2-yl)silyl]oxy}propan-2-ol수율 76.7%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Triisopropylsilyl chloride (83.8 mL, 390 mmol) was added slowly over 15 minutes to a solution of (2R)-propane-1,2-diol (29.7 g, 390 mmol) in DMF at 0° C. (100 mL) keeping the internal temperature below 15° C. This was followed by addition of imidazole (66.4 g, 975 mmol) and the reaction mixture was allowed to warm to RT and stirred under argon for 20 hours. The reaction was quenched with 1M hydrochloric acid/diethyl ether (300 mL/800 mL). The organic layer was separated and washed with 1M hydrochloric acid followed by saturated brine solution. The organic layer was dried (MgSO4), filtered and evaporated. Purification by distillation at 10 mmHg, 90-104° C., afforded the title compound as colourless oil (69.5 g).

후처리

  1. customthe internal temperature below 15° C
  2. customThe reaction was quenched with 1M hydrochloric acid/diethyl ether (300 mL/800 mL)
  3. customThe organic layer was separated
  4. washwashed with 1M hydrochloric acid
  5. dry with materialThe organic layer was dried (MgSO4)
  6. filtrationfiltered
  7. customevaporated
  8. customPurification
  9. distillationby distillation at 10 mmHg, 90-104° C.

출처 및 근거

ORD 기록
ord-dc496a43024a467ebd38497d7b77ea5b
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07745475B2

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