HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578127Generated: October 26, 2026
Diethylamine → 3-(Diethylsulfamoyl)benzoic acid
https://huagongshe.com/reaction/578127
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Benzoic acid, 3-(chlorosulfonyl)- | HCID 77641 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(Diethylsulfamoyl)benzoic acid | HCID 794595 | — |
Reaction Steps
Diethylamine (Aldrich, 2.5 mL, 24 mmol) was added to a solution of 3-(chlorosulfonyl)benzoic acid (Aldrich, 2.0 g, 9.1 mmol) in anhydrous dichloromethane (20 mL) at 0° C. The mixture was then stirred at 0° C. for 2 hours. The volatiles were removed under reduced pressure. The residue was treated with aqueous potassium hydrogensulfate (1 M, 10 mL) and then extracted with ethyl acetate (3×50 mL). The combined extracts were dried over magnesium sulfate filtered and then concentrated to give the title compound. 1H NMR (300 MHz, CD3OD) δ 1.13 (t, J=7.1 Hz, 6H), 3.22-3.30 (m, 4H), 7.69 (t, J=7.8 Hz, 1H), 8.03 (ddd, J=7.9, 1.9, 1.4 Hz, 1H), 8.25 (dt, J=7.8, 1.4 Hz, 1H), 8.40 (t, J=1.7 Hz, 1H) ppm; MS (DCI/NH3) m/z 275 (M+NH4)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040568B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-9344bce09aa34268903a38f8e07eec70 |
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| Source note | uspto-grants-2015_05 |
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