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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566551Generated: October 27, 2026

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

https://huagongshe.com/reaction/566551

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-PropanediolHCID 10442—
ReactantHCID 21266306HCID 21266306—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
Product3-(3,3-Bis(2-methylphenyl)-2-propen-1-yloxy)-1-propanolHCID 1075636331%

Reaction Steps

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 26) 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 (MgSO4) 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174898B1
Source datasetuspto-grants-2001_01
ORD IDord-03b2e68b6968434d95a943f114809173
Source noteuspto-grants-2001_01