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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560164Generated: October 30, 2026

Ethyl Acetate → 5-(2-Benzyloxy-ethyl)-cyclohex-1-enecarboxylic acid methyl ester

https://huagongshe.com/reaction/560164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantThionyl ChlorideHCID 24386—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant5-(2-Benzyloxy-ethyl)-2-hydroxy-cyclohexanecarboxylic acid methyl esterHCID 23549539—
SolventPyridineHCID 1049—
Product5-(2-Benzyloxy-ethyl)-cyclohex-1-enecarboxylic acid methyl esterHCID 23549538—

Reaction Steps

A solution of 5-(2-benzyloxy-ethyl)-2-hydroxy-cyclohexanecarboxylic acid methyl ester (Intermediate R2, 0.72 g, 2.48 mmol) in pyridine (10 mL) was treated with SOCl2 (0.73 mL, 12.4 mmol) at −20 EC. The mixture was allowed to react for 15 m and was then warmed to 55 EC for 16 h. The solvents were removed under vacuum and the residue was diluted in ether at 0 EC. The solution was quenched with water, washed with 1M HCl, 5% NaOH and brine. The organic material was dried over MgSO4 filtered and freed of solvent. The mixture was diluted with benzene and water was removed by azeotropic distillation under vacuum. The residue was dissolved in benzene (15 mL) and DBU (0.76 mL, 5 mmol) was added. The mixture was reacted for 30 m at rt. After work-up and chromatography on SiO2 with 20% EtOAc:Hx 5-(2-benzyloxy-ethyl)-cyclohex-1-enecarboxylic acid methyl ester (Intermediate R3) was isolated 0.56 g (82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063086B2
Source datasetuspto-grants-2011_11
ORD IDord-cf317c62f23847298abdc726d8ffa8fa
Source noteuspto-grants-2011_11