HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197546Generated: October 31, 2026
2-Bromobenzyl bromide → HCID 19107064, compound
https://huagongshe.com/reaction/1197546
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromobenzyl bromide | HCID 76965 | — |
| Reactant | HCID 19107122 | HCID 19107122 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 19107064 | HCID 19107064 | 37% |
Reaction Steps
To a solution of potassium t-butoxide (16.8 g, 0.15 mol) in t-butanol (300 ml) was added methyl 1-benzoyl-4-oxo-3-piperidinecarboxylic acid (36.1 g, 0.146 mol) according to the method of G. Stork, J. Am. Chem. Soc. 68, 1053 (1946). The mixture was stirred 1 hour and 2-bromobenzyl bromide was added dropwise in a solution of t-butanol. The reaction was heated to reflux for 2 days, cooled and filtered. The salts were washed with ether and the organic filtrate was washed with 5% hydrochloric acid (100 ml), saturated sodium bicarbonate (100 ml), water (100 ml) and saturated sodium chloride (100 ml). The organic layer was dried (MgSO4), filtered, and concentrated to yield a crude oil. The material was recrystallized from isopropyl ether to yield a pale yellow solid (23.4 g, 37%) An additional recrystallization produced the title compound a white solid, mp 105°-107° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05276053 |
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| Source dataset | uspto-grants-1994_01 |
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| ORD ID | ord-510c221d0ec74ab586d5aa77b139065b |
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| Source note | uspto-grants-1994_01 |
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