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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989444Generated: October 30, 2026

Cyclohexanone → HCID 12992811, compound

https://huagongshe.com/reaction/989444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantThiazoleHCID 9256—
ReactantAmmonium ChlorideHCID 25517—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
ProductHCID 12992811HCID 1299281168.8%

Reaction Steps

To a solution of n-BuLi (22 mL of a 2.5M solution in hexane, 55 mmol) in anhydrous ether (60 mL) at −78° C. was slowly added a solution of thiazole (3.94 g, 46 mmol) in anhydrous ether (30 mL). The resulting mixture was stirred for 1 h and then cyclohexanone (9.6 mL, 93 mmol) in ether (25 mL) was added over 5 min. The mixture was stirred for 2.5 h at −78° C. and then sat. aq. NH4Cl was added and the phases were separated. The aqueous phase was extracted with ethyl acetate (3×) and the combined organics were washed with water, brine, dried (MgSO4) and concentrated. Flash chromatography of the residue (silica gel; hexane/ethyl acetate 4:1 to 7:3) provided the 2-[(1-Hydroxy)cyclohexyl]thiazole compound (5.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06639077B2
Source datasetuspto-grants-2003_10
ORD IDord-0de22d62f724400eb927229261116200
Source noteuspto-grants-2003_10