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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955035Generated: October 31, 2026

Triethylamine → Ethyl 4-[(methylsulfonyl)amino]butanoate

https://huagongshe.com/reaction/1955035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-Aminobutyrate ethyl hydrochlorideHCID 12649661—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-[(methylsulfonyl)amino]butanoateHCID 5395992394.5%

Reaction Steps

Methanesulfonyl chloride (4.10 g, 35.8 mmol) was added to a suspension of ethyl 4-aminobutyrate hydrochloride (6.00 g, 35.8 mmol) and Et3N (10.8 mL, 77.4 mmol) in THF (230 mL). The resulting suspension was stirred at room temperature for 43 h. The reaction mixture was filtered and the filtrate was concentrated. Flash chromatography (1:1 EtOAc:hexanes to EtOAc) afforded the title compound of Step A (7.08 g). 1H NMR (400 MHz, CDCl3) δ 4.51 (s, 1H), 4.12 (q, 2H), 3.18 (q, 2H), 2.94 (s, 3H), 2.40 (t, 2H), 1.85-1.92 (m, 2H), 1.24 (t, 3H); MS 210 (M+ +1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124314
Source datasetuspto-grants-2000_09
ORD IDord-c0274353a34644c1af936a6c3196813f
Source noteuspto-grants-2000_09