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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722027Generated: October 31, 2026

Benzyl Bromide → HCID 178454070, compound

https://huagongshe.com/reaction/722027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178418329HCID 178418329—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 178454070HCID 178454070—

Reaction Conditions

Temperature70 °C

Reaction Steps

To 6 mL of a tetrahydrofuran solution containing 1.0 g of trans-4-(tert-butoxycarbonylamino)cyclohexanol and 873 mg of benzylbromide was gradually added 204 mg of 60% sodium hydride, 0.5 mL of dimethyl sulfoxide was then further added thereto, and the mixture was stirred at 70° C. for 2 hours. The reaction mixture was poured into water and extracted with chloroform. The extract was washed with water and brine, dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The residue was applied to silica gel column chromatography (solvent: hexane-ethyl acetate (4:1)), and the obtained powdery crystals were suspended in an ethyl acetate-hexane mixed solvent, and collected by filtration to obtain trans-1-tert-butoxycarbonylamino-4-(benzyloxy)cyclohexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138397B2
Source datasetuspto-grants-2006_11
ORD IDord-ce6fada85e99472a97842df9954cd253
Source noteuspto-grants-2006_11