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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665006Generated: October 30, 2026

Pyridine → HCID 67440074, compound

https://huagongshe.com/reaction/1665006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantN-Benzylglycine ethyl esterHCID 80908—
Reactant2-Trifluoromethylbenzenesulphonyl chlorideHCID 136616—
SolventDichloromethaneHCID 6344—
ProductHCID 67440074HCID 6744007462.8%

Reaction Steps

To a stirred solution of 2-trifluoromethylbenzenesulfonyl chloride (3.8 g) in dichloromethane (100 mL) under argon was added pyridine (14 mL). A solution of N-benzylglycine ethylester (2 g) in dichloromethane (40 mL) was added slowly. The mixture was stirred at r.t. overnight and then concentrated under reduced pressure. The residue was dissolved in dichloromethane and washed with water. The organic phase was dried (MgSO4), filtered and concentrated under reduced pressure. The product was purified by chromatography (SiO2, cyclohexane to cyclohexane/ethyl acetate 1:1) to give [benzyl-(2-trifluoromethyl-benzenesulfonyl)-amino]-acetic acid ethyl ester (2.61 g) as a colorless oil. MS: 402.1 ([M+H]+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039493B2
Source datasetuspto-grants-2011_10
ORD IDord-47240197dbca412a9585928b710ef906
Source noteuspto-grants-2011_10