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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015506Generated: October 31, 2026

Acetyl chloride → Methyl 3-acetyltricyclo[3.3.1.03,7]nonane-1-carboxylate

https://huagongshe.com/reaction/1015506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant3-Acetyltricyclo[3.3.1.03,7]nonane-1-carboxylic acidHCID 59374950—
SolventMethanolHCID 887—
ProductMethyl 3-acetyltricyclo[3.3.1.03,7]nonane-1-carboxylateHCID 6701787294.7%

Reaction Steps

To 3-acetyltricyclo[3.3.1.03,7]nonane-1-carboxylic acid (2.4 g, 11.4 mmol) obtained in step I, in MeOH (48 mL) cooled to ice bath temperature, was added acetyl chloride (1.64 mL, 22.8 mmol). The reaction mixture was gradually warmed to room temperature and stirred for 2 h. The volatiles were removed under reduced pressure and the crude product was purified by column chromatography to obtain methyl 3-acetyltricyclo[3.3.1.03,7]nonane-1-carboxylate (2.4 g) in 93% yield as viscous liquid. m/z (M+1) 223. IR cm−1 2953, 1728, 1698, 1461, 1234, 1078, 755. 1H NMR (CDCl3) 300 MHz δ 3.66 (s, 3H), 2.75-2.70 (m, 1H), 2.53-2.46 (m, 1H), 2.40-2.32 (m, 1H), 2.19 (s, 3H), 2.15-2.05 (m, 1H), 2.03-1.60 (m, 8H). 13C NMR (CDCl3) 75 MHz δ 210.9, 175.3, 61.4, 53.4, 51.6, 50.5, 48.0, 45.9, 45.6, 42.6, 41.9, 36.8, 35.9, 26.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985759B2
Source datasetuspto-grants-2011_07
ORD IDord-605c889d938246c6b715e3d4e5ae5057
Source noteuspto-grants-2011_07