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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500079Generated: October 28, 2026

Water → HCID 178444563, compound

https://huagongshe.com/reaction/500079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSilanamine, 1,1,1-trimethyl-N-(trimethylsilyl)-, potassium saltHCID 45051783—
ReactantHCID 53261455HCID 53261455—
ReactantHCID 178453953HCID 178453953—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 178444563HCID 17844456367%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a mixture of 5-butylsulfonyl-1-phenyl-1H-tetrazole (3.54 g) and anhydrous ethylene glycol dimethyl ether (60 ml) at −60° C. was added 0.5 M hexamethyldisilazane potassium solution (in toluene, 26.6 ml), and the mixture was stirred for 20 minutes. Under the same condition, a solution of t-butyl cis-4-formylcyclohexylcarbamate (3.02 g) in anhydrous ethylene glycol dimethyl ether (15 ml) was added to the mixture. And the reaction mixture was gradually warmed to 25° C. and stirred overnight. To the reaction mixture was added water, and the mixture was stirred for 1 hour, then extracted with diethyl ether, and the organic layer was washed with brine, dried over sodium sulfate, and then the solvent was removed in vacuo. The residue was purified by a silica gel chromatography (eluent: gradient from 100% hexane/0% ethyl acetate to 0% hexane/100% ethyl acetate) to give 2.38 g of t-butyl cis-{4-[(E)-1-pentenyl]cyclohexyl}carbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767854B2
Source datasetuspto-grants-2010_08
ORD IDord-c7bd9161aa24401eb5079031fbaee68c
Source noteuspto-grants-2010_08