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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168030Generated: October 25, 2026

Water → methyl N-(3-phenylbenzyl)N-(2-propynyl)carbamate

https://huagongshe.com/reaction/1168030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPropargyl bromideHCID 7842—
ReactantSodium hydrideHCID 24758—
Reactantmethyl N-(3-phenylbenzyl)carbamateHCID 12090300—
SolventTetrahydrofuranHCID 8028—
Productmethyl N-(3-phenylbenzyl)N-(2-propynyl)carbamateHCID 1209030566.6%

Reaction Steps

0.70 g of methyl N-(3-phenylbenzyl)carbamate in tetrahydrofuran (20 ml) was stirred together with 0.15 g of 60% sodium hydride at room temperature for 30 minutes. 0.52 g of propargyl bromide was added dropwise at room temperature, and the resulting solution was stirred overnight. After the reaction, the reaction solution was poured into water and extracted with ethyl acetate, and the organic layer was separated, dried over anhydrous magnesium sulfate and evaporated under reduced pressure for removal of the solvent. The residue was purified by silica gel column chromatography to give 0.54 g of methyl N-(3-phenylbenzyl)N-(2-propynyl)carbamate as a yellow transparent viscous liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620961B1
Source datasetuspto-grants-2003_09
ORD IDord-2cc273e41362477eac54574d2e47ddc6
Source noteuspto-grants-2003_09