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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397609Generated: October 29, 2026

Triethylamine → HCID 54075416, compound

https://huagongshe.com/reaction/397609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 23000869HCID 23000869—
SolventDichloromethaneHCID 6344—
ProductHCID 54075416HCID 5407541677.2%

Reaction Steps

0.77 g (7.6 mmol) of triethylamine were added to a 20 ml methylene chloride solution of 1.86 g (7.6 mmol) of the 1-(t-butoxycarbonyl)-3-(1-hydroxyethyl)-4-piperidone obtained above. Under ice cooling, 0.88 g (7.6 mmol) of methanesulfonyl chloride were added and the resulting mxiture was stirred at room temperature for 1 hour. The solvent was distilled off under reduced pressure. Ethyl acetate was added to the residue. The solid thus precipitated was filled out, followed by concentration under reduced pressure again. The concentrate was then dissolved in 20 ml of chloroform, followed by the addition of 1.16 g (7.6 mmol) of 1,8-diazabicyclo[5.4.0]under-7-ene (DBU) at room temperature. The mixture was stirred for 2 hours at the same temperature. After completion of the reaction, the reaction mixture was concentrated under reduced pressure. The residue was subjected to chromatography on a silica gel column (eluting solvent: toluene/ethyl acetate=19/1), whereby 1.32 g (yield: 77.2%) of the title compound were obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610708B1
Source datasetuspto-grants-2003_08
ORD IDord-675c486cee6a4c54bcaf36b66032c479
Source noteuspto-grants-2003_08