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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201754Generated: October 28, 2026

tert-Butyl N-(2-bromoethyl)carbamate → HCID 71003970, compound

https://huagongshe.com/reaction/2201754

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl N-(2-bromoethyl)carbamateHCID 4103526—
ReactantHCID 71003969HCID 71003969—
SolventAcetonitrileHCID 6342—
ProductHCID 71003970HCID 7100397074%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 3-benzyl-5-hydroxyisoindolin-1-one (360 mg, 1.51 mmol), CsCO3 (980 mg, 3.01 mmol) and tert-butyl 2-bromoethylcarbamate (506 mg, 2.26 mmol) in 4 mL of acetonitrile was heated up to 80° C. for 4 hours, TLC showed complete conversion. The solvent was evaporated and the residue was dissolved in ethyl acetate, then water was added, this was separated. The organic phase was dried on Na2SO4 and the solvent was evaporated. The residue was purified by flash-chromatography on silica gel with 100% ethyl acetate, 426 mg (1.11 mmol, 74%) of the product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365512B2
Source datasetuspto-grants-2016_06
ORD IDord-fb39a51ca5f84d31a08dca718676538e
Source noteuspto-grants-2016_06