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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423087Generated: October 31, 2026

Ethanol → tert-butyl N-[2-amino-1-(4-chlorophenyl)ethyl]carbamate

https://huagongshe.com/reaction/423087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium AzideHCID 33557—
Reactant2-(Tert-butoxycarbonylamino)-2-(4-chlorophenyl)ethyl methanesulfonateHCID 57750278—
CatalystPalladiumHCID 23938—
SolventDimethylformamideHCID 6228—
Producttert-butyl N-[2-amino-1-(4-chlorophenyl)ethyl]carbamateHCID 5775038699%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 2-(tert-butoxycarbonylamino)-2-(4-chlorophenyl)ethyl methanesulfonate (Intermediate 23) (535 mg, 1.53 mmol) in DMF (8 mL) was treated with sodium azide (199 mg, 3.06 mmol) and the mixture was heated at 80° C. for 1 hour. The mixture was cooled and allowed to stir at room temperature overnight. The solution was partitioned between ethyl acetate and water. The organic layer was washed twice with water then dried with magnesium sulfate, filtered and concentrated until the final volume was approximately 5 mL. Ethanol (20 mL) and 10% palladium on carbon (75 mg, 0.07 mmol) were added. The resulting suspension was stirred under an atmosphere of hydrogen at ambient pressure and temperature for 1 hour. The mixture was filtered and the filtrate was concentrated under reduced pressure to give tert-butyl 2-amino-1-(4-chlorophenyl)ethylcarbamate as a gum (410 mg, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101623B2
Source datasetuspto-grants-2012_01
ORD IDord-32c5a0e8da454e40985b831be5d49397
Source noteuspto-grants-2012_01