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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198306Generated: November 1, 2026

Water → HCID 19103907, compound

https://huagongshe.com/reaction/1198306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Cyclopenten-1-oneHCID 13588—
Reactant1-Bromo-4-tert-butylbenzeneHCID 77595—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
SolventHCID 19103921HCID 19103921—
ProductHCID 19103907HCID 19103907—

Reaction Steps

A solution of 34 g of 4-t-butylphenylbromide (0.16 mole) in 50 ml diethyl ether was slowly added to a stirred mixture of 100 ml of a solution of n-butyllithium in hexane (1.6 mole/l) and 50 ml diethyl ether, while the temperature of the mixture was kept at -25 ° C. After completion of the addition, the temperature of the resultant mixture was allowed to rise slowly to about room temperature. Subsequently the temperature was decreased to -25° C. and 13.2 g of 2-cyclopentene-1-one (0.16 mole) dissolved in a small volume of diethyl ether was slowly added. The suspension thus obtained, was allowed to reach room temperature and then stirred for one hour. An excess amount of water was added to the suspension to result in 1-(4-t-butylphenyl)cyclopentanol. The 1-(4-t-butylphenyl)cyclopent-2-en-1-ol product was isolated from the reaction mixture by extraction with diethyl ether and subsequently purified by chromatography over silica, using dichloromethane as the elution solvent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05279999
Source datasetuspto-grants-1994_01
ORD IDord-9f5d92752c2f4e96a284553dfc04dbc0
Source noteuspto-grants-1994_01