Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444767Generated: October 30, 2026

Ammonia → ETHYL 2-(1-HYDROXYCYCLOBUTYL)ACETATE

https://huagongshe.com/reaction/444767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantEthyl bromoacetateHCID 7748—
ReactantCyclopentanoneHCID 8452—
CatalystZincHCID 23994—
SolventDiethyl EtherHCID 3283—
ProductETHYL 2-(1-HYDROXYCYCLOBUTYL)ACETATEHCID 5813484054.1%

Reaction Steps

Trimethylchlorosilane (1.14 mL, 8.92 mmol) was added by syringe to a suspension of zinc powder (7.97 g, 0.122 mol) in absolute Et2O (200 mL). The mixture was stirred for 15 minutes at room temperature. The mixture was then heated to reflux, the heat source was removed, and ethyl bromoacetate (10.3 mL, 92.9 mmol) was added at such a rate that the ether solution gently boiled. The mixture was refluxed one hour then stirred for an additional hour at room temperature. A solution of cyclopentanone (6.00 g, 75.9 mmol) in ether (30 mL) was added while the temperature of the mixture was maintained at 19-20° C. by intermittent cooling. After being one hour of stirring at room temperature, the mixture was poured into iced 25% ammonia (400 mL). The aqueous phase was extracted with ether and the combined phases were dried over K2CO3. Filtration and evaporation of the solvent yielded the title compound as a colorless oil (6.50 g, 54%). 1H-NMR (400 MHz, CDCl3) δ 1.29 (3H, t, J=7.3 Hz), 1.47-1.64 (1H, m), 1.76-1.87 (1H, m), 1.93-2.06 (2H, m), 2.12-2.22 (2H, m), 2.67 (2H, s), 3.70 (1H, s), 4.19 (2H, q, J=7.3 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476261B2
Source datasetuspto-grants-2013_07
ORD IDord-7e328153f7e74ceb9262d7e1c4078c79
Source noteuspto-grants-2013_07