HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359952Generated: October 31, 2026
4-Bromobenzyl bromide → HCID 66961148, compound
https://huagongshe.com/reaction/1359952
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (3R)-pyrrolidin-3-ol hydrochloride | HCID 2759336 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66961148 | HCID 66961148 | 71% |
Reaction Steps
Diisopropylethylamine (1.57 ml, 9.00 mmol) was added to a solution (15 ml) of 1.50 g (6.00 mmol) of 4-bromobenzyl bromide and 1.11 g (9.00 mmol) of (R)-pyrrolidin-3-ol hydrochloride in dimethylformamide and the mixture was stirred at room temperature for one hr. The solvent was removed by distillation under the reduced pressure. Water and 1 N hydrochloric acid were then added to the residue, and the mixture was washed with ethyl acetate. A 5 N aqueous sodium hydroxide solution and an aqueous sodium hydrogencarbonate solution were added thereto, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate and was then filtered. The filtrate was concentrated under the reduced pressure to give 1.09 g (yield 71%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07879808B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-092760c553d7494bbf8d78ca14994d80 |
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| Source note | uspto-grants-2011_02 |
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