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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839261Generated: October 28, 2026

Benzenesulfonyl chloride → Nonyl [(benzenesulfonyl)oxy]carbamate

https://huagongshe.com/reaction/839261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
Reactant1,4-DioxaneHCID 31275—
ReactantNonyl hydroxycarbamateHCID 21314104—
SolventWaterHCID 962—
ProductNonyl [(benzenesulfonyl)oxy]carbamateHCID 54340962—

Reaction Conditions

Temperature25 °C

Reaction Steps

20.4 Parts of triethylamine are added to a stirred mixture of 40.6 parts of nonyl-N-hydroxycarbamate, 100 parts of dioxan and 35.3 parts of benzene sulphonyl chloride at 0° C keeping the pH in the range 2 to 5. The mixture is stirred for 18 hours at 25° C then added to 500 parts of water. The oily product is separated into 300 parts of toluene and the solution is washed with water, dried and evaporated at 40° l C under reduced pressure to give 72 parts of nonyl-N-benzenesulphonyloxycarbamate as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04094863
Source datasetuspto-grants-1978_06
ORD IDord-270a5b0e176441af9e5ceeab05d5c476
Source noteuspto-grants-1978_06