HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486794Generated: October 31, 2026
Benzenesulfonyl chloride → HCID 118006539, compound
https://huagongshe.com/reaction/1486794
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | 1-Amino-3,3-diethoxypropane | HCID 521029 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 118006539 | HCID 118006539 | — |
Reaction Steps
To a suspension of sodium carbonate (31 g, 0.37 mol) in water (50 ml) was added a solution of 1-amino-3,3-diethoxypropane (10.00 mL, 61.81 mmol) in DCM (50 mL) followed by cooling to 0° C. benzenesulfonyl chloride (7.65 mL, 60.0 mmol) was added at 0° C. with vigorous stirring followed by warming to 20° C. and continued stirring for 2 h after which time MTBE (150 mL) was added. Organic layer was separated, washed with 1.0 M of HCl (50 mL), saturated NaHCO3 (50 g), water (50 g), concentrated and azeotroped to dry two times with MTBE (150 mL×2) to provide N-(3,3-diethoxypropyl)benzenesulfonamide, 28 (17.34 g, 60.34 mmol, 97% yield) as light yellow clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428495B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-044659ce79e24ad289fe83c2e257a7ab |
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| Source note | uspto-grants-2016_08 |
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