HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239746Generated: October 26, 2026
Tramiprosate → 3-Pivaloylamino-1-propanesulfonic acid
https://huagongshe.com/reaction/239746
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tramiprosate | HCID 1646 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Pivaloylamino-1-propanesulfonic acid | HCID 11123727 | — |
Reaction Steps
3-amino-1-propanesulfonic acid (2.0 g, 14.4 mmol) was dissolved a NaOH (1.2 g, 30.2 mmol) solution in a mixture of 1,4-dioxane (5 mL) and water (15 mL). The mixture was cooled to 0° C. before pivaloyl chloride (2.8 mL, 21.6 mmol) in 1,4-dioxane (5 mL) was added dropwise. The reaction mixture was allowed to warm up to room temperature and it was stirred at 65° C. for 4 h. The solvent was evaporated under reduced pressure. The resulting solid was dissolved in water (30 mL), and treated with Dowex 50WX8 resin. The suspension was stirred for 5 minutes and the resin was removed by filtration. The filtrate was evaporated under reduced pressure. The residual material was suspended in 20% EtOH/Acetone. The mixture was stirres at reflux for 30 seconds. The solid product was collected by filtration, and dried in vacuo, to afford compound DT (1.3 g, 41%). 1H NMR (D2O, 500 MHz) δ ppm 3.16 (t, 2H, J=6.8 Hz), 2.75 (t, 2H, J=7.8 Hz), 1.78 (m, 2H), 1.1 (s, 9H). 13C NMR (D2O, 125 MHz) δ ppm 182.75, 48.70, 38.57, 38.18, 26.65, 24.27. ES-MS 222 (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-cf155817470f46eca12c9d6bb7f3133d |
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| Source note | uspto-grants-2014_02 |
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