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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133164Generated: October 25, 2026

Hexamethylphosphoramide → 5-(2-Benzyloxy-ethyl)-2-oxo-cyclohexanecarboxylic acid methyl ester

https://huagongshe.com/reaction/133164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexamethylphosphoramideHCID 12679—
ReactantCarbonocyanidic acid, methyl esterHCID 28660—
ReactantLithium diisopropylamideHCID 2724682—
Reactant4-(2-Benzyloxyethyl)cyclohexanoneHCID 21879605—
SolventTetrahydrofuranHCID 8028—
Product5-(2-Benzyloxy-ethyl)-2-oxo-cyclohexanecarboxylic acid methyl esterHCID 5744324390%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of LDA (33 ml, 1.5 M in Et2O) (available from Aldrich) in THF (50 mL) at −78° C. was treated with 4-(2-benzyloxy-ethyl)-cyclohexanone (9.5 g, 40.2 mmol). The mixture was warmed to 0° C. over 30 m before re-cooling to −78° C. and adding HMPA (7 mL). Methyl cyanoformate (4.1 mL, 85 mmol) (available from Aldrich) was added and the mixture was stirred for 15 m before aqueous quench and work-up. The product was purified by chromatography on SiO2 with 10% EtOAc:Hx. 5-(2-Benzyloxy-ethyl)-2-oxo-cyclohexanecarboxylic acid methyl ester was isolated, 5.8 g (49%) and reduced with an equivalent of NaBH4 in MeOH at −10° C. The alcohol (Intermediate A2) was purified by chromatography on SiO2 with 30 to 50% EtOAC:Hx. (−90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390829B2
Source datasetuspto-grants-2008_06
ORD IDord-53fc676723b54bdcb3daaee9c35b50f8
Source noteuspto-grants-2008_06