Lithium borohydride → (R)-Benzyl (1,5-dihydroxypentan-2-yl)carbamate

HRID 7286

반응식

HRID 7286 반응식
[CH2:1]([O:8][C:9]([NH:11][CH:12]([CH2:16][CH2:17][C:18]([O-])=[O:19])[C:13]([O-])=[O:14])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[BH4-].[Li+]>C1COCC1.[Cl-].[Na+].O.O>[OH:19][CH2:18][CH2:17][CH2:16][C@@H:12]([NH:11][C:9](=[O:10])[O:8][CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)[CH2:13][OH:14]

참가 물질

6

반응물 2

HCID 4148881Lithium borohydrideHCID 22017142[((Benzyloxy)carbonyl]amino}pentanedioate

생성물 1

HCID 2757382(R)-Benzyl (1,5-dihydroxypentan-2-yl)carbamate수율 81.2%

시약·촉매·용매 3

HCID 962Water용매HCID 8028Tetrahydrofuran용매2회HCID 57417360Sodium chloride; water용매

실험 절차

A solution of dimethyl (2R)-2-{[((benzyloxy)carbonyl]amino}pentanedioate (22.4 g) in dry THF (74 ml) was added dropwise over 1 h to a stirred mixture of lithium borohydride (4.5 g) in THF (200 ml) at room temperature, under nitrogen. Stirring at room temperature was continued for 3 days. The reaction mixture was diluted with brine and water, and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried (over magnesium sulphate) and concentrated under reduced pressure to give the title compound (16.5 g) as a white solid.

후처리

  1. extractionextracted with ethyl acetate
  2. washThe combined organic extracts were washed with brine
  3. dry with materialdried (over magnesium sulphate)
  4. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-0716b8127315465ca5bb1dda1907bd78
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07084139B2

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