Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1183083Generated: November 1, 2026

Triethylamine → HCID 52872884, compound

https://huagongshe.com/reaction/1183083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Nitrobenzenesulfonyl chlorideHCID 15540—
ReactantN-Boc-N-methylethylenediamineHCID 2756424—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 52872884HCID 5287288470.4%

Reaction Steps

2-Nitrobenzenesulfonyl chloride (4.9 g, 22 mmol) was added to a dichloromethane solution (100 ml) of tert-butyl (2-aminoethyl)methylcarbamate (3.5 g, 20 mmol) and triethylamine (3.3 ml, 24 mmol) at 0° C., and stirred at room temperature overnight. Water was added to the reaction mixture, and extraction with dichloromethane was performed. The organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:2→2:3). The purified product was concentrated under reduced pressure to thereby obtain 5.06 g (yield: 70%) of tert-butyl methyl-[2-(2-nitrobenzenesulfonylamino)ethyl]carbamate as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664217B2
Source datasetuspto-grants-2014_03
ORD IDord-1b0ceb853cfb43e08b09635777fc9d77
Source noteuspto-grants-2014_03