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Water → HCID 69155444, 화합물

HRID 1836908
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HRID 1836908 반응식
[Br:1][C:2]1[C:11]([CH3:12])=[CH:10][C:9]2[C:8]([CH3:14])([CH3:13])[CH:7]=[CH:6][C:5]([CH3:16])([CH3:15])[C:4]=2[CH:3]=1.S(=O)(O)[O-:18].[Na+].[OH2:22]>N1C=CC=CC=1.[Os](=O)(=O)(=O)=O>[Br:1][C:2]1[C:11]([CH3:12])=[CH:10][C:9]2[C:8]([CH3:14])([CH3:13])[C@@H:7]([OH:22])[C@@H:6]([OH:18])[C:5]([CH3:16])([CH3:15])[C:4]=2[CH:3]=1
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참가 물질

6

반응물 3

HCID 962WaterHCID 109568496-Bromo-1,1,4,4,7-pentamethyl-1,4-dihydronaphthaleneHCID 23665763Sodium Bisulfite

생성물 1

HCID 69155444HCID 69155444, 화합물수율 75%

시약·촉매·용매 2

HCID 30318Osmium Tetroxide촉매HCID 1049Pyridine용매

실험 절차

To a solution of 9.41 g (33.7 mmol) of 2-bromo-3,5,5,8,8-pentamethyl-5,8-dihydronaphthalene in 110 ml pyridine was added 8.65 g (34.0 mmol) osmium tetroxide under an atmosphere of nitrogen. After stirring at room temperature for 18 hours, 17.3 g (166 mmol) of sodium bisulfite in 110 ml water was added. After 2 hours the resulting solution was partitioned between ethyl acetate and aqueous hydrochloric acid. The organic layer was washed with water, washed with brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. The crude material was purified by flash chromatography with elution with 30% ethyl acetate/hexane to yield 7.97 g (75%) of 2-bromo-cis-6,7-dihydroxy-3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalene as a white solid (M+=312).

후처리

  1. customAfter 2 hours the resulting solution was partitioned between ethyl acetate and aqueous hydrochloric acid
  2. washThe organic layer was washed with water
  3. washwashed with brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated in vacuo
  6. customThe crude material was purified by flash chromatography with elution with 30% ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-7179cd60538e46cd89603f9e9f883d28
출처 데이터셋
uspto-grants-2004_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06777418B2

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