5-Bromohex-1-ene → HCID 86683230, compound

To magnesium turnings (7.44 g, 0.020 moles) in dry THF (100 mL) and was added a iodine (100 mg) at room temperature. To this reaction mass was added a solution of 5-bromohex-1-ene (50 g, 362 mmoles) in THF (200 mL). The reaction mass was heated with hot air gun to initiate the reaction. Upon completion of the reaction the solution was transferred by cannula to a solution of (S)-propylene oxide (14 g, 241 mmol) and copper bromide (3.45 g, 24 mmol) in THF (100 mL) at −78° C. The reaction mass was allowed to come to room temperature and was stirred overnight. The reaction mass was quenched with saturated aq. ammonium chloride solution and extracted with diethyl ether (200 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated at room temperature to get crude compound. The crude compound was purified by column chromotography (Silica gel, 10% TBME in pet ether) to get (2S)-4-methyloct-7-en-2-ol (12.4 g, 30%) as an oil. 1H NMR (400 MHz, CDCl3): δ ppm 5.84-5.77 (m, 1H), 5.02-4.92 (m, 2H), 4.05-3.85 (sb, 1H), 2.08-2.06 (m, 2H), 1.29-1.20 (m, 2H), 1.19-1.16 (m, 4H), 0.97-0.87 (m, 6H).

1. temperatureThe reaction mass was heated with hot air gun
2. customthe reaction
3. customUpon completion of the reaction the solution
4. customto come to room temperature
5. customThe reaction mass was quenched with saturated aq. ammonium chloride solution
6. extractionextracted with diethyl ether (200 mL×3)
7. dry with materialThe combined organic layers were dried over anhydrous Na2SO4
8. concentrationconcentrated at room temperature
9. customto get crude compound
10. customThe crude compound was purified by column chromotography (Silica gel, 10% TBME in pet ether)

ORD record

ord-2e41adf559ab4e07a9c793ab4416fc60

Source dataset

uspto-grants-2015_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08957203B2