HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253005Generated: October 25, 2026
Triethylamine → (S)-N-(1-Hydroxybutan-2-yl)-2-nitrobenzenesulfonamide
https://huagongshe.com/reaction/253005
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Nitrobenzenesulfonyl chloride | HCID 15540 | — |
| Reactant | 2-Amino-1-butanol, (+)- | HCID 120084 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-N-(1-Hydroxybutan-2-yl)-2-nitrobenzenesulfonamide | HCID 66861496 | 99.1% |
Reaction Steps
Triethylamine (0.94 ml, 6.74 mmol) was added to a solution of 400 mg (4.49 mmol) of (S)-2-aminobutan-1-ol in tetrahydrofuran (5 ml), and the mixture was stirred at room temperature for 10 min. 2-Nitrobenzenesulfonyl chloride (995.1 mg, 4.49 mmol) was added to the solution, and the mixture was stirred at room temperature for 15 min. A saturated aqueous sodium hydrogencarbonate solution was added thereto to stop the reaction, and the reaction solution was then extracted with ethyl acetate, was dried over anhydrous sodium sulfate, and was filtered. The filtrate was concentrated under the reduced pressure, and the residue was purified by column chromatography on silica gel (hexane:ethyl acetate=2:1) to give 1.22 g (yield 99%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07871982B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-561b8a09e87945bf98599213f9276bfa |
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| Source note | uspto-grants-2011_01 |
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