1,3-Propanediol → 3-(3,3-Bis(2-methylphenyl)-2-propen-1-yloxy)-1-propanol

HRID 1614824Notes

Reaction equation

HRID 1614824 reaction equation
C([Li])CCC.[CH2:6]([OH:10])[CH2:7][CH2:8][OH:9].Br[CH2:12][CH:13]=[C:14]([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=1[CH3:28])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[CH3:21]>O>[CH3:28][C:23]1[CH:24]=[CH:25][CH:26]=[CH:27][C:22]=1[C:14]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[CH3:21])=[CH:13][CH2:12][O:9][CH2:8][CH2:7][CH2:6][OH:10]

Participants

5

Reactant 3

HCID 104421,3-PropanediolHCID 21266306HCID 21266306, compoundHCID 178418339Butyllithium

Product 1

HCID 107563633-(3,3-Bis(2-methylphenyl)-2-propen-1-yloxy)-1-propanolYield 31%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

A solution of n-butyllithium in hexanes (15.2 ml, 2.5 M) was added dropwise under a nitrogen atmosphere to 1,3- propanediol (31 ml) on an ice-bath. When addition was complete the mixture was stirred 0.5 h at room temperature. 3-Bromo-1,1-bis(2-methylphenyl)-1-propene (11.5 g, 38 mmol, prepared in a similar way to the method described in Example 23) was added and the reaction mixture was stirred at room temperature for 48 h and at 75° C. for 36 h. Water (100 ml) was added and the mixture was extracted with ethyl acetate (100 ml). The phases were separated and the organic phase was washed with water (2×50 ml), dried over magnesium sulphate and the solvent evaporated in vacuo. Flash chromatography of the residue on silica gel (300 g) using a gradient of n-heptane in ethyl acetate as eluent provided 3.5 g (31 %) of 3-(3,3-bis(2-methyl phenyl)-2-propen-1-yloxy)-1-propanol.

Workup

  1. additionWhen addition
  2. additionwas added
  3. stirringthe reaction mixture was stirred at room temperature for 48 h and at 75° C. for 36 h
  4. extractionthe mixture was extracted with ethyl acetate (100 ml)
  5. customThe phases were separated
  6. washthe organic phase was washed with water (2×50 ml)
  7. dry with materialdried over magnesium sulphate
  8. customthe solvent evaporated in vacuo

Sources & evidence

ORD record
ord-9b6d29ce56f04f2fac26e9db761ff461
Source dataset
uspto-grants-1993_03
Patent number
US05198451

Reaction notes

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