Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789644Generated: October 31, 2026

Linalool → 3-(2,4-Dihydroxyphenyl)-acrylic acid 1,5-dimethyl-1-vinyl-hex-4-enyl ester

https://huagongshe.com/reaction/1789644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLinaloolHCID 6549—
ReactantTriethylamineHCID 8471—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant3-(2,4-dihydroxyphenyl)prop-2-enoic AcidHCID 3359493—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product3-(2,4-Dihydroxyphenyl)-acrylic acid 1,5-dimethyl-1-vinyl-hex-4-enyl esterHCID 66933240—

Reaction Steps

To a solution of linalool (1.74 g, 11.3 mmol) and triethylamine (2.30 g, 22.6 mmol) in anhydrous THF (150 mL) stirred for 5 min at 22° C. is added 3-(2,4-dihydroxyphenyl)-acrylic acid (2.04 g, 11.3 mmol). To this heterogeneous solution is added BOP Reagent (5.00 g, 11.3 mmol; Aldrich #22,608-4) in DMF (10 mL), and the subsequent homogeneous reaction mixture is stirred for 1 h. The reaction mixture is partitioned between ether (200 mL) and water (400 mL); the organic layer is removed and washed with ether (200 mL). The combined organic layers are washed sequentially with saturated sodium bicarbonate solution (200 mL) and brine (200 mL). The organic layer is dried over anhydrous magnesium sulfate, vacuum filtered and concentrated to give 3-(2,4-dihydroxyphenyl)-acrylic acid 1,5-dimethyl-1-vinyl-hex-4-enyl ester as an oil that is purified by flash chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071151B2
Source datasetuspto-grants-2006_07
ORD IDord-fc60b71ab90445cab311ed1798fa62bf
Source noteuspto-grants-2006_07