Oxygen → 1-Phenyl-3-heptanol

HRID 650325Notes

Reaction equation

HRID 650325 reaction equation
[BH3-]C#N.[Na+].C([OH:9])(C)(C)C.I[CH:11]([CH2:20][CH2:21][CH2:22][CH3:23])[CH2:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.O=O>O.CC(N=NC(C#N)(C)C)(C#N)C>[C:14]1([CH2:13][CH2:12][CH:11]([OH:9])[CH2:20][CH2:21][CH2:22][CH3:23])[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1

Participants

7

Procedure

A reaction vessel (50 ml, a two-neck, eggplant type flask) is subjected to nitrogen gas purging. NaBH3CN (1.0 mmol, 62.8 mg), AIBN (0.005 mmol, 0.8 mg) and Bu2(t-Bu)SnCl (0.025 mmol, 8.1 mg, 7 μl) are added to tert-butanol (2 ml). Then, 3-iodo-1-phenylheptane (0.5mmol, 151.1mg, 115 μl) is added. The introduction of nitrogen gas is discontinued, a nitrogen gas-filled black butyl rubber balloon is set instead, and using a syringe, oxygen (0.75 mmol, 18 ml) is bubbled into the solution. Thereafter, the reaction vessel is immersed in an oil bath at 60° C. After 13 hours, heating is discontinued and the reaction mixture is diluted with pure water (10 ml) and extracted with ether (15 ml×4). The organic solution is dried over anhydrous magnesium sulfate and the solvent is distilled off. The residue is purified by column chromatography (silica gel 4 g, ethyl acetate/hexane 20%) to provide 1phenyl-3-heptanol (89.4 mg, 93%).

Workup

  1. customA reaction vessel (50 ml, a two-neck, eggplant type flask) is subjected to nitrogen gas
  2. custompurging
  3. customThereafter, the reaction vessel is immersed in an oil bath at 60° C
  4. temperatureheating
  5. extractionextracted with ether (15 ml×4)
  6. dry with materialThe organic solution is dried over anhydrous magnesium sulfate
  7. distillationthe solvent is distilled off
  8. customThe residue is purified by column chromatography (silica gel 4 g, ethyl acetate/hexane 20%)

Sources & evidence

ORD record
ord-d1ff557505c2425189f70ba2ceb664d5
Source dataset
uspto-grants-2001_08
Patent number
US06271425B1

Reaction notes

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