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Hydrochloric Acid → tert-butyl 3-[(1S)-1-hydroxypropyl]benzoate

HRID 554763
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HRID 554763 반응식
C(N(CCCC)[C@H:6]([CH3:15])[C@H:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[OH:8])CCC.C(C1C=C(C=CC=1)[C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])=O.C([Zn]CC)C.[Cl-].[NH4+].Cl>C1(C)C=CC=CC=1.CCCCCC>[OH:8][C@H:7]([C:9]1[CH:10]=[C:11]([CH:12]=[CH:13][CH:14]=1)[C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])[CH2:6][CH3:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 5

HCID 313Hydrochloric AcidHCID 25517Ammonium ChlorideHCID 10845940Tert-butyl 3-formylbenzoateHCID 11003877(1S,2R)-(-)-2-(Dibutylamino)-1-phenyl-1-propanolHCID 178418750HCID 178418750, 화합물

생성물 1

HCID 66934833tert-butyl 3-[(1S)-1-hydroxypropyl]benzoate수율 1,950.8%

시약·촉매·용매 2

HCID 1140Toluene용매HCID 8058Hexane용매2회

실험 절차

To the (1S,2R)-2-di-n-butylamino-1-phenyl-1-propanol (200 mg) in toluene (7 ml) solution, tert-butyl 3-formylbenzoate (3 g) in hexane (7 ml) solution was added and the mixture was stirred at room temperature for 20 minutes. Next, diethylzinc in 1N hexane solution (33 ml) was added to the reaction solution under ice cooling and the mixture was stirred at that temperature for 18 hours. Saturated ammonium chloride aqueous solution was added to the reaction solution, the mixture was stirred at 20 minutes, and 1N hydrochloric acid was added. The obtained mixed solution was extracted with ethyl acetate. The organic layer was dried over with anhydrous sodium sulfate, then concentrated to obtain the title compound (3.5 g).

후처리

  1. stirringthe mixture was stirred at that temperature for 18 hours
  2. stirringthe mixture was stirred at 20 minutes
  3. additionThe obtained mixed solution
  4. extractionwas extracted with ethyl acetate
  5. dry with materialThe organic layer was dried over with anhydrous sodium sulfate
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-4dbc5cbd72634134ac7205d2db6ee9f9
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08049006B2

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