Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328357Generated: October 25, 2026

Benzyl Chloride → N-benzyl-N-mesyl-O-(p-methoxybenzyl)hydroxylamine

https://huagongshe.com/reaction/328357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantN-mesyl-O-(p-methoxybenzyl)hydroxylamineHCID 12763343—
SolventSodium MethoxideHCID 10942334—
ProductN-benzyl-N-mesyl-O-(p-methoxybenzyl)hydroxylamineHCID 1276334465.6%

Reaction Steps

9.25 g (40 mmoles) of N-mesyl-O-(p-methoxybenzyl)hydroxylamine prepared as described in Reference Example 5 was added to sodium methoxide (prepared from 150 ml of absolute methanol and 1.2 g of sodium metal), and 6 g of benzyl chloride was then added to the mixture. The resulting mixture was heated under refluxing for 3 hours. The solvent was distilled off, and 150 ml of ethyl acetate and 50 ml of water were added to the residue. The organic layer was separated, dried over anhydrous sodium sulfate and concentrated to obtain 8.4 g (65.6% yield) of N-benzyl-N-mesyl-O-(p-methoxybenzyl)hydroxylamine having a melting point of 85°-87° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04017512
Source datasetuspto-grants-1977_04
ORD IDord-90c6fd5f3d2b45739de7ce4eb390ee8f
Source noteuspto-grants-1977_04