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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propane sultone | HCID 14264 | — |
| Reactant | Valinamide | HCID 445637 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[(1S)-1-carbamoyl-2-methylpropyl]amino-1-propanesulfonic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642801B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-b1a263d1898344c590f940a3368082d5 |
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| Source note | uspto-grants-2014_02 |
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