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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292592Generated: November 1, 2026

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

https://huagongshe.com/reaction/2292592

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 into 100 ml of anhydrous DMF at 0° C., and 51.6 g (0.25 mol) of the compound from Example XX in 250 ml of anhydrous 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 anhydrous DMF are added dropwise at 5°-15° C. and the mixture is stirred at 25° C. for 20 h. After concentrating, the residue is partitioned between water and 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 numberUS05684014
Source datasetuspto-grants-1997_11
ORD IDord-90f22fb698fd47aea3e56dcc4f3ec7bc
Source noteuspto-grants-1997_11