Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210561Generated: October 31, 2026

Bromocyclopentane → Tert-butyl 2-cyclopentyl-2-(4-methylphenyl)acetate

https://huagongshe.com/reaction/2210561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromocyclopentaneHCID 8728—
Reactanttert-Butyl (4-methylphenyl)acetateHCID 12362014—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 2-cyclopentyl-2-(4-methylphenyl)acetateHCID 15234721—

Reaction Conditions

Temperature0 °C

Reaction Steps

33.5 g (0.3 mol) of potassium tert-butoxide are initially introduced at 0° C. into 100 ml of DMF with exclusion of moisture, and 51.6 g (0.25 mol) of tert-butyl 4-methylphenylacetate in 250 ml of DMF are added dropwise. The mixture is stirred at 0° C. for 30 min and 32.2 ml (0.3 mol) of cyclopentyl bromide in 150 ml of DMF are added dropwise at 5°-15° C. and the mixture is stirred at 25° C. for 20 h. After concentration, the residue is partitioned between water/diethyl ether, and the ether phase is dried over sodium sulphate and concentrated. The product crystallizes out.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05459156
Source datasetuspto-grants-1995_10
ORD IDord-1d4db8f04b2d44cbb432382e18074a17
Source noteuspto-grants-1995_10