HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882588Generated: November 2, 2026
Dibromodifluoromethane → (2S,3E)-1,4-diphenylbut-3-en-2-amine
https://huagongshe.com/reaction/882588
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dibromodifluoromethane | HCID 6382 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Alumina | HCID 9989226 | — |
| Reactant | (2S)-1-(benzylsulphonyl)-3-phenylpropan-2-amine | HCID 68310878 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (2S,3E)-1,4-diphenylbut-3-en-2-amine | HCID 68309085 | — |
Reaction Steps
552.7 mg (9.85 mmol) of potassium hydroxide were dissolved in methanol, adsorbed onto 1.1 g of neutral aluminium oxide and then dried under high vacuum. To a solution of 240 mg (0.82 mmol) of (2S)-1-(benzylsulphonyl)-3-phenylpropan-2-amine and 1.56 g of the potassium hydroxide on aluminium oxide thus prepared in 6.2 ml of n-butanol were added dropwise, at 5-10° C., 307 μl (3.3 mmol) of dibromodifluoromethane. The reaction mixture was stirred at RT for 2 h, then filtered through Celite, and the residue was washed thoroughly with dichloromethane. The filtrate was concentrated and the resulting residue was dried under reduced pressure. The crude product thus obtained was purified by means of preparative HPLC. 98 mg (35% of theory) of the title compound were obtained with an E/Z diastereomer ratio of 4:1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08992932B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-2a756f9b74224f8093ddb93c0dac91ed |
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| Source note | uspto-grants-2015_03 |
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