Water → HCID 22992380, compound

HRID 2259993Notes

Reaction equation

HRID 2259993 reaction equation
[Cl:1][C:2]1[C:3]([CH:16](O)[CH3:17])=[CH:4][C:5]2[C:6]([CH3:15])([CH3:14])[CH2:7][CH2:8][C:9]([CH3:13])([CH3:12])[C:10]=2[CH:11]=1.P(Br)(Br)[Br:20].O.[C:24]1([P:30]([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)[C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>CCOCC.CCCCCC>[Br-:20].[Cl:1][C:2]1[C:3]([CH:16]([P+:30]([C:31]2[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=2)([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)[C:24]2[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=2)[CH3:17])=[CH:4][C:5]2[C:6]([CH3:15])([CH3:14])[CH2:7][CH2:8][C:9]([CH3:13])([CH3:12])[C:10]=2[CH:11]=1

Participants

7

Procedure

To a solution of 3.15 g (11.8 mmol) of (±)-1-(3-chloro-5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalen-2-yl) ethanol in ether and hexane stirring at 0° C. under argon, was added dropwise 31.9 g (11.2 mL, 118 mmol) of phosphorus tribromide and the mixture stirred 1.5 hours. Water was then carefully added and the mixture extracted with several portions of ether. The ether extracts were washed with water, sodium bicarbonate, brine, and dried (MgSO4). The solvent was removed in-vacuo and the residual oil taken up in 175 mL of benzene. To this was added 3.09 g (11.8 mmol) of triphenylphosphine and the solution stirred for 24 hours at room temperature. Purification was done using flash chromatography (SiO2, 0.5% ethyl acetate in hexanes, 5% MeOH in methylene chloride) to give the title compound as a white foam.

Workup

  1. extractionthe mixture extracted with several portions of ether
  2. washThe ether extracts were washed with water, sodium bicarbonate, brine
  3. dry with materialdried (MgSO4)
  4. customThe solvent was removed in-vacuo
  5. stirringthe solution stirred for 24 hours at room temperature
  6. customPurification

Sources & evidence

ORD record
ord-42a612ca13d54225b35f1cbda18a53ba
Source dataset
uspto-grants-1995_12
Patent number
US05475113

Reaction notes

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