HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264449Generated: October 30, 2026
N-Acetylsulfanilyl chloride → HCID 18552221, compound
https://huagongshe.com/reaction/1264449
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Acetylsulfanilyl chloride | HCID 8481 | — |
| Reactant | 3-Bromopropylamine hydrobromide | HCID 78701 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18552221 | HCID 18552221 | 166.7% |
Reaction Steps
To a stirred solution of N-acetylsulfanilyl chloride (57.15 g, 0.244 mol) in acetone (500 mL) and H2O (187.5 mL) at 0° C. was added 3-bromopropylamine hydrobromide (25.0 g, 0.114 mol). When a clear solution was obtained, a solution of sodium hydrogencarbonate (44.15 g, 0.526 mol) in H2O (550 mL) was added dropwise, maintaining the internal temperature at 0-5° C. When the addition was completed, the reaction mixture was heated at 50° C. for 5 h, then cooled to room temperature and poured into ice H2O with stirring. After stirring at 5° C. for 4 h, the suspension was filtered and the filter cake was washed with H2O and dried in vacuo to give 34.6 g (90%). An additional reaction was performed to give an additional 63.7 g of similar material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06544499B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-d423130fef2d42b095e0a06a772435ff |
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| Source note | uspto-grants-2003_04 |
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