Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842751Generated: November 1, 2026

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

https://huagongshe.com/reaction/842751

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 numberUS06376502B1
Source datasetuspto-grants-2002_04
ORD IDord-7303c7beeb86437da7cd6c567b2aeb53
Source noteuspto-grants-2002_04