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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299619Generated: November 1, 2026

2-Bromopropane → HCID 57129610, compound

https://huagongshe.com/reaction/2299619

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropaneHCID 6358—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 57157362HCID 57157362—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 57129610HCID 57129610—

Reaction Steps

Under nitrogen, to dimethylsulfoxide (3 ml) was added potassium hydroxide (31 mg) at room temperature, and the suspension was stirred at the same temperature for 1 hour. To this one were added N-(3-hydroxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-yl)-N-[(2S)-3-phenoxy-2-(triethylsilyloxy)propyl]-tert-butoxycarbonylamine (150 mg) and isopropyl bromide (78 μl), and the mixture was stirred at room temperature for 3 hours. The resulting mixture was poured into aqueous 10% sodium hydrogencarbonate, and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate =20:1) to give N-(3-isopropoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-yl)-N-[(2S)-3-phenoxy-2-(triethylsilyloxy)propyl]-tert-butoxycarbonylamine (96 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495546B1
Source datasetuspto-grants-2002_12
ORD IDord-d1ed423f00ca4be8b74bba37b4135a90
Source noteuspto-grants-2002_12