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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154439Generated: October 30, 2026

Cyclohexanol → HCID 53848100, compound

https://huagongshe.com/reaction/1154439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanolHCID 7966—
ReactantHCID 54532449HCID 54532449—
CatalystTitanium(IV)ethoxideHCID 2724286—
SolventPotassium FluorideHCID 522689—
ProductHCID 53848100HCID 53848100—

Reaction Steps

12 g (26.6 mmol) of tert.butyl (S)-12,12a-dihydro-8-iodo-9-oxo-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carboxylate, 70 ml (660 mmol) of cyclohexanol and 2 g (8 mmol) of tetraethyl orthotitanate are stirred at 120° overnight, the solution is evaporated to dryness and the residue is taken up in chloroform. The solution obtained is stirred for 0.5 hour with 120 ml of a saturated potassium fluoride solution, the resulting emulsion is filtered through siliceous earth, the organic phase is separated, washed with water, dried over magnesium sulphate and evaporated. By crystallization from ethyl acetate and hexane there is obtained cyclohexyl (S)-12,12a-dihydro-8-iodo-9-oxo-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carboxylate of melting point 124°-125°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04489003
Source datasetuspto-grants-1984_12
ORD IDord-fa13f76bf100471590a8c372df2d440f
Source noteuspto-grants-1984_12