Pentane → HCID 68650155, compound

HRID 1771871Notes

Reaction equation

HRID 1771871 reaction equation
Br[C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[O:9][CH3:10].[Li][C:12]([CH3:15])(C)[CH3:13].CCCCC.C1C[O:24]CC1>>[F:8][C:6]1[CH:5]=[CH:4][C:3]([O:9][CH3:10])=[C:2]([CH2:13][C@H:12]([OH:24])[CH3:15])[CH:7]=1

Participants

5

Conditions

Temperature
-78 °C

Procedure

A solution of 2-bromo-4-fluoro-1-methoxybenzene (2.0 g, 9.75 mmol) in 20 mL of anhydrous THF was cooled to −78° C. Then 1.7M solution of t-BuLi in pentane (13.0 mL, 22.1 mmol) was added dropwise. The mixture was stirred at −78° C. for 10 min, then R-(+)-propylene oxide (670 mg, 11.55 mmol) was added and the mixture was allowed to warm to 0° C. overnight. The mixture was quenched with 2 mL of sat. NH4Cl and then conc. HCl was added dropwise to pH 8. The mixture was extracted with EtOAc (2×20 mL), the extract was dried over Na2SO4 and evaporated to give crude oil, which was purified by column (silicagel, EtOAc/hexane 1:9) to give (2R)-1-(5-fluoro-2-methoxyphenyl)propan-2-ol (531 mg, 30%). 1H NMR (300 MHz, CDCl3): δ 6.88 (m, 2H), 6.78 (m, 1H), 4.06 (m, 1H), 3.81 (s, 3H), 2.66-2.84 (m, 2H), 1.92 (d, J=3.96 Hz, 1H), 1.22 (d, J=6.21 Hz, 3H).

Workup

  1. temperatureto warm to 0° C. overnight
  2. customThe mixture was quenched with 2 mL of sat. NH4Cl
  3. additionconc. HCl was added dropwise to pH 8
  4. extractionThe mixture was extracted with EtOAc (2×20 mL)
  5. dry with materialthe extract was dried over Na2SO4
  6. customevaporated
  7. customto give crude oil, which
  8. customwas purified by column (silicagel, EtOAc/hexane 1:9)

Sources & evidence

ORD record
ord-ab0af2e91d2145068146583dd9a22a75
Source dataset
uspto-grants-2016_02
Patent number
US09249147B2

Reaction notes

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