HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17172Generated: October 25, 2026
Carbon tetrabromide → (S)-t-butyl 2-(2,2-dibromovinyl)pyrrolidine-1-carboxylate
https://huagongshe.com/reaction/17172
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-Boc-2-Formylpyrrolidine | HCID 4227815 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-t-butyl 2-(2,2-dibromovinyl)pyrrolidine-1-carboxylate | HCID 14730281 | 86% |
Reaction Steps
A solution of triphenylphosphine (21.1 g, 80.3 mmol) and carbon tetrabromide (13.32 g, 40.16 mmol) in dichloromethane (300 mL) at 0° C. was treated with a solution of 2-formyl -pyrrolidine-1-carboxylic acid tert-butyl ester (4.0 g, 20.08 mmol) in dichloromethane (10 mL) dropwise via syringe. The solution was stirred for 1 hour at room temperature, poured into a saturated sodium bicarbonate solution and separated. The organic phase was dried (MgSO4), filtered and concentrated. The concentrate was purified by flash chromatography on silica gel using 0-1% methanol/dichloromethane to give 6.13 g (86% yield) of the desired product. 1H NMR (300 MHz, CHLOROFORM-D) δ ppm 1.47 (s, 9H), 1.81 (m, 3H), 2.16 (m, 1H), 3.39 (m, 2H), 4.37 (s, 1H), 6.38 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737160B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-282782dd16794bb7bdd7cd11cc6d17f7 |
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| Source note | uspto-grants-2010_06 |
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