2-Methyl-3-tert.-butoxypropan-1-ol → 1-Bromo-3-tert-butoxy-2-methylpropane
Reaction equation
[C:1]([O:5][CH2:6][CH:7]([CH3:10])[CH2:8]O)([CH3:4])([CH3:3])[CH3:2].[Br:11]Br.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>>[C:1]([O:5][CH2:6][CH:7]([CH3:10])[CH2:8][Br:11])([CH3:4])([CH3:3])[CH3:2]Participants
3
Procedure
Reaction of rac.-3-tert. butoxy-2-methyl-1-propanol with bromine-triphenylphosphine using the procedure of Example 28 gave rac.-3-tert. butoxy-2-methyl-1-bromopropane in 35% yield as a colorless liquid, b.p. 67°-77° C. (bath temperature) (9 mm Hg.).
Sources & evidence
- ORD record
- ord-b09300400c234f3ea01375a8a01cdf55
- Source dataset
- uspto-grants-1980_03
- Patent number
- US04191842
Reaction notes
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