Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280803Generated: October 31, 2026

Ammonia → 2-Phenylbicyclo[1.1.1]pentane

https://huagongshe.com/reaction/2280803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSodiumHCID 5360545—
Reactant2-Phenylbicyclo[1.1.1]pentan-2-yl acetateHCID 10035745—
SolventDiethyl EtherHCID 3283—
Product2-Phenylbicyclo[1.1.1]pentaneHCID 1105179493%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 2-phenylbicyclo[1.1.1]pentan-2-yl acetate (2.7 g, 13.4 mol) in 50 mL of anhydrous ether was placed in a three-necked flask. The flask was cooled to −78° C., and 150 mL of liquid ammonia was added. To the stirring mixture was added sodium (0.62 g, 27.0 mmol) in small pieces over a period of 10 minutes. Stirring was continued until the blue color was discharged. The reaction was quenched by the addition of saturated aqueous ammonia chloride solution (5 mL), and the solvent was allowed to evaporate overnight. Pentane (40 mL) was added to the residue, and the solution was washed with 30 mL saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated. The crude product was purified by column chromatography (100% pentane) to give the desired compound as a colorless liquid (1.8 g, 12.5 mmol, yield: 93%). 1H NMR (300 MHz, CDCl3) δ ppm 7.40-7.21 (m, 5H), 3.48 (d, J=6.9 Hz, 1H), 2.81 (s, 2H), 2.20 (dd, J1=9.9 Hz, J2=2.7 Hz, 1H), 2.00 (d, J=2.1 Hz, 1H), 1:94-1.85 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139534B2
Source datasetuspto-grants-2015_09
ORD IDord-ef7aed5c98d246bf8bbce723529d9b07
Source noteuspto-grants-2015_09