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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991767Generated: November 2, 2026

Methanol → Methyl 3-acetyladamantane-1-carboxylate

https://huagongshe.com/reaction/991767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Methoxycarbonyladamantane-1-carboxylic Acid ChlorideHCID 54178337—
ReactantHCID 178418348HCID 178418348—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDiethyl EtherHCID 3283—
ProductMethyl 3-acetyladamantane-1-carboxylateHCID 21940569—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Under nitrogen, a chilled (0° C.) diethyl ether suspension of copper (1) iodide (3.0 eq) was treated with methyl lithium (6.0 eq, 1.4 M in ethyl ether). The resulting solution was chilled to −78° C. and after ten minutes a chilled (−30° C.) diethyl ether solution of 3-methoxycarbonyladamantane-1-carboxylic acid chloride was added dropwise over a five minute period. The reaction was stirred for 45 minutes at −78° C. and then quenched with MeOH (11.0 eq) and allowed to warm to room temperature. After addition of Et2O and saturated aqueous ammonium chloride solution, the mixture was stirred for ten minutes and then the organic phase was washed with saturated NH4Cl, saturated NaHCO3, brine, dried (MgSO4), filtered and concentrated to a volatile oil, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06465513B1
Source datasetuspto-grants-2002_10
ORD IDord-91f61e29c0a5432aa21de1ca42c8d205
Source noteuspto-grants-2002_10