Acetone → 2-(4-Aminophenyl)propan-2-ol

HRID 2241961Notes

Reaction equation

HRID 2241961 reaction equation
Br[C:2]1[CH:7]=[CH:6][C:5](/[N:8]=N/N2CCCC2)=[CH:4][CH:3]=1.[Li]C(CC)C.[CH3:20][C:21]([CH3:23])=[O:22]>CCOCC>[NH2:8][C:5]1[CH:4]=[CH:3][C:2]([C:21]([OH:22])([CH3:23])[CH3:20])=[CH:7][CH:6]=1

Participants

5

Conditions

Temperature
-78 °C

Procedure

To a −78° C. solution of compound 134 (1 g, 3.95 mmol) in ether (20 mL) was added sec-BuLi (1.4 M in hexanes, 0.62 g, 9.67 mmol). The resulting solution was stirred for 30 min at −78° C., followed by addition of acetone (0.91 g, 15.81 mmol) dropwise at −78° C. The reaction mixture was warmed to room temperature overnight. The reaction mixture was partitioned between water and ether and the layers were separated. The aqueous layer was re-extracted with ether. The ether layers were the combined and concentrated in vacuo to yield crude 135 (0.33 g, 55.9%) which was used in the next step without further purification.

Workup

  1. temperatureThe reaction mixture was warmed to room temperature overnight
  2. customThe reaction mixture was partitioned between water and ether
  3. customthe layers were separated
  4. extractionThe aqueous layer was re-extracted with ether
  5. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-03f2e67ef35845359a9e152f478a50a6
Source dataset
uspto-grants-2010_03
Patent number
US07671061B2

Reaction notes

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