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Sodium Azide → (3S,5R)-3-Azidomethyl-5-methyl-octanoic acid tert-butyl ester

HRID 1374196
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HRID 1374196 반응식
[C:1]([O:5][C:6](=[O:27])[CH2:7][C@@H:8]([CH2:15]OS(C1C=CC(C)=CC=1)(=O)=O)[CH2:9][C@H:10]([CH3:14])[CH2:11][CH2:12][CH3:13])([CH3:4])([CH3:3])[CH3:2].[N-:28]=[N+:29]=[N-:30].[Na+]>CS(C)=O.O>[C:1]([O:5][C:6](=[O:27])[CH2:7][C@@H:8]([CH2:15][N:28]=[N+:29]=[N-:30])[CH2:9][C@H:10]([CH3:14])[CH2:11][CH2:12][CH3:13])([CH3:4])([CH3:3])[CH3:2]
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참가 물질

5

반응물 2

HCID 33557Sodium AzideHCID 57178500(3S,5R)-5-Methyl-3-(toluene-4-sulfonyloxymethyl)-octanoic Acid Tert-butyl Ester

생성물 1

HCID 57060687(3S,5R)-3-Azidomethyl-5-methyl-octanoic acid tert-butyl ester수율 79%

시약·촉매·용매 2

HCID 679Dimethyl Sulfoxide용매HCID 962Water용매

실험 절차

Tosylate 104 (2.92 g, 7.3 mmol) and sodium azide (1.43 g, 0.02 mol) were warmed to ˜50° C. in DMSO (30 mL). After 2 hours the solution was cooled to room temperature and diluted with water. The solution was extracted with ether and the combined organic phases dried (MgSO4) and concentrated to give an oil 1.54 g, 79%. Further purification by flash chromatography (95% hexane/EtOAc) gave an oil. [α]D=−8.3 (c 1 in CHCl3). 13C NMR (100 MHz; CDCl3) 172.01, 80.73, 54.89, 39.73, 39.46, 39.00, 33.40, 29.85, 28.30, 20.15, 19.82, 14.52.

후처리

  1. extractionThe solution was extracted with ether
  2. dry with materialthe combined organic phases dried (MgSO4)
  3. concentrationconcentrated

출처 및 근거

ORD 기록
ord-c1e9e935296540dda94570720518bc93
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07164034B2

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