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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249894Generated: October 27, 2026

Benzyl chloroformate → (1-Methoxymethyl-propyl)-carbamic acid benzyl ester

https://huagongshe.com/reaction/2249894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Butanamine, 1-methoxy-HCID 93837—
Solvent1,4-DioxaneHCID 31275—
Product(1-Methoxymethyl-propyl)-carbamic acid benzyl esterHCID 6688910176%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1-methoxymethyl-propylamine (2.50 g, 24.3 mmol, 1.0 eq.) in dioxane (15 mL) was added an aqueous solution of K2CO3 (15 g in 15 mL of H2O) and the mixture was cooled to 0° C. CBZ-Cl (4.16 mL, 1.2 eq.) was then introduced and the resulting mixture was warmed to room temperature and stirred for 3 h, extracted with EtOAc. The combined organicphase was dried over Na2SO4, filtered and concentrated. The residue was purified by chromatography (hexanes to 40% EtOAc/hexanes) to give (1-methoxymethyl-propyl)-carbamic acid benzyl ester (4.4 g, 76%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314936B2
Source datasetuspto-grants-2008_01
ORD IDord-93a3182aabbc46b8845bd2dd05606787
Source noteuspto-grants-2008_01