HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504305Generated: October 31, 2026
4-Bromophenacyl bromide → HCID 58209525, compound
https://huagongshe.com/reaction/1504305
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromophenacyl bromide | HCID 7454 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (4S)-1-(tert-Butoxycarbonyl)-4-methyl-L-proline | HCID 26596883 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 58209525 | HCID 58209525 | — |
Reaction Steps
To a mixture of p-bromophenacyl bromide (242 mg, 0.87 mmol) in DCM (1.5 mL) and DMA (1.5 mL), under nitrogen, was added (2S,4S)-4-methyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester (200 mg, 0.87 mmol) and N,N-diisopropylethylamine (531.8 μL, 3.05 mmol) and the resulting mixture was stirred at 35° C. for 3 h, concentrated under vacuum, dissolved in DCM (30 mL), and washed with water (2×5 ml). The organic layer was dried over magnesium sulfate, filtered, and concentrated under vacuum to provide the title intermediate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09212168B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-62a46e6b23ee4bdfbc8d16a0641a016a |
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| Source note | uspto-grants-2015_12 |
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