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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239752Generated: October 27, 2026

Propane sultone → 3-[(1S)-1-carbamoyl-2-methylpropyl]amino-1-propanesulfonic acid

https://huagongshe.com/reaction/239752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropane sultoneHCID 14264—
ReactantValinamideHCID 445637—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-[(1S)-1-carbamoyl-2-methylpropyl]amino-1-propanesulfonic acidHCID 16035842—

Reaction Steps

To a solution of L-valinamide (1.57 g, 13.5 mmol) in tetrahydrofuran (20 mL) was slowly added 1,3-propane sultone (1.61 g, 12.9 mmol). The mixture was stirred at reflux for 2 hours. The reaction mixture was cooled to room temperature. The solid material was collected by filtration, washed with acetone (2×25 mL). The crude product was dissolved in water (60 mL) and treated with ion exchange resin Dowex Marathon C (strongly acidic, 15 g). The mixture was stirred for 15 minutes. The resin was removed by filtration. The filtrate was poured into EtOH (250 mL). The solid product, after the completion of the precipitation, was collected by filtration, and dried in vacuo, to afford compound EQ (1.6 g, 51%). 1H NMR (D2O, 500 MHz) δ ppm 3.63 (d, 1H), 3.05 (m, 2H), 2.85 (m, 2H), 2.05 (m, 4H), 0.93 (d, 3H), 0.88 (d, 3H). 13C NMR (D2O, 125 MHz) δ ppm 170.24, 65.92, 48.16, 46.31, 29.59, 21.31, 18.02, 17.07. [α]D=+10.5° (c=0.0027 in water), ES-MS 237 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642801B2
Source datasetuspto-grants-2014_02
ORD IDord-b1a263d1898344c590f940a3368082d5
Source noteuspto-grants-2014_02