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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506750Generated: October 30, 2026

Triethylamine → N-(benzyloxycarbonyl)-4-(mesyloxy)butylamine

https://huagongshe.com/reaction/1506750

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantBenzyl N-(4-hydroxybutyl)carbamateHCID 3366758—
SolventTetrahydrofuranHCID 8028—
ProductN-(benzyloxycarbonyl)-4-(mesyloxy)butylamineHCID 1114114581.3%

Reaction Conditions

Temperature22.5 °C

Reaction Steps

To a solution of benzyl 4-hydroxybutylcarbamate (1.1 g, 4.9 mmol) and triethylamine (1.7 mL, 9.8 mmol) in THF was added methanesulfonyl chloride (0.67 g, 5.9 mmol) at 0° C. The reaction was stirred at 20-25° C. for 6 hours and concentrated. The residue was partitioned between ethyl acetate and water. The phases were separated, and the organic layer was washed with hydrochloride solution (1 N), saturated sodium bicarbonate solution, and saline. The separated organic layer was dried and concentrated to give 4-(benzyloxycarbonylamino)butyl methanesulfonate (1.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221760B2
Source datasetuspto-grants-2015_12
ORD IDord-b20122d48fe34482a3c16ad8d8803456
Source noteuspto-grants-2015_12