HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894366Generated: October 29, 2026
Benzhydrylamine → 3-Chloro-propane-1-sulfonic acid benzhydryl-amide
https://huagongshe.com/reaction/1894366
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzhydrylamine | HCID 7036 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Chloropropanesulphonyl chloride | HCID 15410 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Chloro-propane-1-sulfonic acid benzhydryl-amide | HCID 43653836 | 118.6% |
Reaction Steps
In a three-neck round bottom flask equipped with argon inlet was charged with anhydrous tetrahydrofuran and 3-chloropropane sulfonyl chloride (500 mg, 2.82 mmol, Aldrich). The flask was cooled down to 0° C., and aminodiphenylmethane (0.49 mL, 2.82 mmol, Fluka) was added, followed by triethylamine (0.59 mL, 4.23 mmol). The reaction mixture was stirred at 0° C. and monitored by the thin layer chromatography. Upon completion, water was added the reaction mixture. It was concentrated then diluted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated to give 3-chloro-propane-1-sulfonic acid benzhydryl-amide (1.083 g, light brown solid). The crude product was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513239B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-34c7f4a9864a49a5bc04c5f02675cac3 |
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| Source note | uspto-grants-2013_08 |
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