gamma-Propanol → 4-(3-Hyd-roxypropyl)-2-t-butylphenol
Reaction equation
[C:1]([C:5]1[CH:6]=[C:7]([CH2:16][CH2:17][CH2:18][OH:19])[CH:8]=[C:9](C(C)(C)C)[C:10]=1[OH:11])([CH3:4])([CH3:3])[CH3:2]>FC(F)(F)C(O)=O>[C:1]([C:5]1[CH:6]=[C:7]([CH2:16][CH2:17][CH2:18][OH:19])[CH:8]=[CH:9][C:10]=1[OH:11])([CH3:4])([CH3:2])[CH3:3]Participants
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A stirred solution of III (12.5 Kg) in trifluoroacetic acid (60.0 L) was heated 40° C. for 6 hrs. After completion of reaction on TLC, reaction mixture was quenched in ice-water and extracted 3 times with dichloromethane (25.0 L). Total organic layers were combined and evaporated to dryness at atmospheric pressure. A solution of sodium hydroxide (3.0 Kg) in methanol (50.0 L) was added to the residue and stirred at room temperature for 1 hr. The solution was neutralized with 1N HCl and extracted 3 times with dichloromethane (25.0 L). All the organic layers were combined and washed with saturated sodium carbonate solution (10.0 L), DM Water (10.0 L), brine (10.0 L) and evaporated to dryness under reduced pressure to give the title compound (7.5 Kg)
Workup
- customAfter completion of reaction
- customon TLC, reaction mixture
- customwas quenched in ice-water
- extractionextracted 3 times with dichloromethane (25.0 L)
- customevaporated to dryness at atmospheric pressure
- additionA solution of sodium hydroxide (3.0 Kg) in methanol (50.0 L) was added to the residue
- extractionextracted 3 times with dichloromethane (25.0 L)
- washwashed with saturated sodium carbonate solution (10.0 L), DM Water (10.0 L), brine (10.0 L)
- customevaporated to dryness under reduced pressure
Sources & evidence
- ORD record
- ord-ebba5e16d5fc49b6b9e9838f05b3786e
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07825257B1
Reaction notes
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