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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495801Generated: October 26, 2026

Ammonium Chloride → tert-Butyl 2-hydroxy-2-methylpropylcarbamate

https://huagongshe.com/reaction/495801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 2-((tert-butoxycarbonyl)amino)acetateHCID 357729—
ReactantTetrahydrofuran tolueneHCID 22635083—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 2-hydroxy-2-methylpropylcarbamateHCID 1110612933.7%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Ethyl 2-(tert-butoxycarbonylamino)acetate (4.17 g, 20.52 mmol) was dissolved in tetrahydrofuran (60 ml). The solution was cooled to −78° C. A 22% solution of methyl magensium chloride in toluene/tetrahydrofuran (purchased from Chemmetallgesellschaft, 27.1 ml, 67.72 mmol) was added dropwise. The reaction mixture was stirred for 1.5 h at −78° C. and then warmed to room temperature. A 10% aqueous solution of ammonium chloride (200 ml) was added dropwise. The phases were separated. The aqueous phase was extracted with ethyl acetate (3×100 ml). The combined organic layers were washed with saturated sodium hydrogen carbonate solution (200 ml) and dried over magnesium sulfate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (110 g), using ethyl acetate/heptane (1:1) as eluent, to give 1.31 g of 2-hydroxy-2-methylpropylcarbamic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939880B2
Source datasetuspto-grants-2005_09
ORD IDord-85f0ff331f0a41d388ba933a4774a419
Source noteuspto-grants-2005_09