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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17171Generated: October 25, 2026

Iodoethane → tert-butyl N-ethyl-N-(prop-2-yn-1-yl)carbamate

https://huagongshe.com/reaction/17171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
Reactanttert-butyl N-(prop-2-yn-1-yl)carbamateHCID 11073648—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Producttert-butyl N-ethyl-N-(prop-2-yn-1-yl)carbamateHCID 1836615147%

Reaction Steps

A suspension of sodium hydride (354 mg, 14.2 mmol) in DMF (33 mL) at room temperature was treated with a solution of Example 516A (2.0 g, 12.9 mmol) in DMF (10 mL) and stirred for one hour at room temperature. The solution was cooled to 0° C., treated with ethyl iodide (1.24 mL, 15.5 mmol), stirred for one hour at 0° and overnight at room temperature. The solution was diluted with water (25 mL), extracted with diethyl ether (2×50 mL) and the combined organic layers were washed with brine (30 mL0, dried (MgSO4), filtered and concentrated. The residue was purified by flash chromatography on silica gel using 5-10% ethyl acetate/hexanes to give the 1.1 g (47% yield) of the desired product. MS (ESI(+)) m/e 184 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737160B2
Source datasetuspto-grants-2010_06
ORD IDord-093ae3d4bbe64e2187e00394a517fbec
Source noteuspto-grants-2010_06