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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440703Generated: October 30, 2026

Triethylamine → 1,1-Dimethylethyl (((2,4,6-trimethylphenyl)sulphonyl)oxy)carbamate

https://huagongshe.com/reaction/440703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Mesitylenesulfonyl chlorideHCID 13046—
Reactanttert-butyl N-hydroxycarbamateHCID 97534—
SolventDiethyl EtherHCID 3283—
Product1,1-Dimethylethyl (((2,4,6-trimethylphenyl)sulphonyl)oxy)carbamateHCID 35928569.5%

Reaction Steps

A stirred solution of 25.0 grams (0.114 mole) of 2,4,6-trimethylbenzenesulfonyl chloride and 15.3 grams (0.114 mole) of 1,1-dimethylethyl N-hydroxycarbamate in 350 mL of diethyl ether was cooled in an ice-water bath, and 11.4 grams (0.114 mole) of triethylamine was added dropwise. Upon completion of the addition, the reaction mixture was allowed to warm to ambient temperature as it stirred for about 18 hours. The reaction mixture was then filtered, and the filtrate was concentrated under reduced pressure to a residue, which was slurried with toluene and petroleum ether. The resultant solid was collected by filtration, yielding 25.0 grams of 1,1-dimethylethyl N-(2,4,6-trimethylphenylsulfonyloxy)carbamate. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521147
Source datasetuspto-grants-1996_05
ORD IDord-eacf51e1a654425e8eb05774c51177d5
Source noteuspto-grants-1996_05