HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970899Generated: October 30, 2026
Hydrochloric Acid → HCID 22601342, compound
https://huagongshe.com/reaction/970899
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | HCID 16788272 | HCID 16788272 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22601342 | HCID 22601342 | — |
Reaction Steps
To solution of 3-[(Pyridin-2-ylmethyl)-sulfamoyl]-benzoic acid (840 mg, 2.87 mmol) in THF (5 ml) was added BH3.THF (1M, 14.4 ml, 14.4 mmol) dropwise. After the addition, the reaction mixture was allowed to stir for 18 h at room temperature, and 5 N HCl (8 ml) was carefully added, resulting in the evolution of H2. Upon heating to 70° C. for 2 h, a clear solution was obtained. Water (30 ml) was added, and the resulting solution was extracted with diethyl ether (3×20 ml). The aqueous phase was cooled to 0° C., neutralized with solid NaOH, and then solid NaHCO3 and extracted with CHCl3 (6×20 ml). The combined organic extracts were dried over MgSO4, and concentrated under reduced pressure. The crude material was used without further purification in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07312234B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-59419663d56341ae8a8973c044e1060a |
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| Source note | uspto-grants-2007_12 |
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