HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351689Generated: October 30, 2026
4-Fluorobenzenesulfonyl chloride → HCID 22713308, compound
https://huagongshe.com/reaction/351689
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| Reactant | Cyclopropanemethanamine | HCID 75646 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22713308 | HCID 22713308 | 88.2% |
Reaction Steps
To a stirred solution of 2 mL (23 mmol) of aminomethyl cyclopropane in 25 mL methylene chloride was added 4.8 mL (28 mmol) of diisopropylethyl amine. After 10 minutes of stirring, 4.49 g (23 mmol) of 4-fluorobenzene sulfonyl chloride was added and the mixture was allowed to stir for 4 hours. The reaction mixture was quenched with water and the organic layer was washed twice with 1N HCl, twice with water, dried over magnesium sulfate and then concentrated in vacuo. Then the solid was dried under vacuum to give 4.65 g of the title compounds as an off white solid; 1H NMR (CDCl3) δ 0.08-0.13 (m, 2H), 0.45-0.51 (m, 2H), 0.83-0.94 (m, 1H), 2.86 (t, J=6.9 Hz, 2H), 4.66-4.71 (m, 1H), 7.12-7.23 (m, 2H), 7.85-7.92 (m, 2H); MS (ES) m/z 218.23 (MH+); HRMS for C10H12FNO2S: 218.0637
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06743787B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-f5e1f0c855e74838817b708248607d76 |
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| Source note | uspto-grants-2004_06 |
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