HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715672Generated: October 30, 2026
Benzyl Bromide → HCID 178525078, compound
https://huagongshe.com/reaction/715672
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178511566 | HCID 178511566 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178525078 | HCID 178525078 | 102.8% |
Reaction Steps
cis-4-Aminocyclohexanecarboxylic acid (10.0 g, 67.48 mmol) was dissolved in 140 mL of dry acetonitrile. Solid potassium carbonate (28.0 g, 202.6 mmol) was added. The suspension was heated to about 80° C. To this solution, was added benzyl bromide (28.09 mL, 236.2 mmol) in 70 mL of acetonitrile, dropwise via addition funnel. The reaction mixture was stirred at about 80° C. under nitrogen for about 2 hours then about 40° C. overnight. The reaction was cooled to room temperature and the suspension was filtered. The filtrate was concentrated under reduced pressure. The compound was purified using column chromatography on silica gel (100% hexanes to remove excess benzyl bromide, then 10% ethyl acetate in hexanes). The product was isolated as a white solid (14.35 g, 51% yield): ES-MS (m/z) 414.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187479B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-88350d5f4a2f4f54b985bb42bf75c331 |
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| Source note | uspto-grants-2015_11 |
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