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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168031Generated: October 26, 2026

Water → methyl N-methoxymethyl-N-(3-phenylbenzyl)carbamate

https://huagongshe.com/reaction/1168031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantBromomethyl methyl etherHCID 83093—
Reactantmethyl N-(3-phenylbenzyl)carbamateHCID 12090300—
SolventTetrahydrofuranHCID 8028—
Productmethyl N-methoxymethyl-N-(3-phenylbenzyl)carbamateHCID 1209030676.1%

Reaction Steps

1.00 g of methyl N-(3-phenylbenzyl)carbamate in tetrahydrofuran (20 ml) was stirred together with 0.22 g of 60% sodium hydride at room temperature for 30 minutes. 0.78 g of methoxymethyl 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 0.90 g of methyl N-methoxymethyl-N-(3-phenylbenzyl)carbamate as a pale yellow transparent viscous liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620961B1
Source datasetuspto-grants-2003_09
ORD IDord-a241719dc28248dcb5e7c404b29c52ec
Source noteuspto-grants-2003_09