HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715669Generated: October 26, 2026
Benzyl Bromide → HCID 178525079, compound
https://huagongshe.com/reaction/715669
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | HCID 178511567 | HCID 178511567 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178525079 | HCID 178525079 | 99% |
Reaction Steps
To an 80° C. heated mixture of trans-4-Aminocyclohexanecarboxylic acid (8 g, 55.97 mmol) and K2C03 (23.4 g) in 112 mL of CH3CN, was added dropwise a solution of BnBr (23.3 mL, 195.5 mmol) in 70 mL of CH3CN by addition funnel. Reaction stirred overnight at 80° C. The reaction was cooled to room temperature and filtered. Precipitate did not form in filtrate like it did with the cis-somer so the filtrate was concentrated to an oil and carried on to next step (23.01 g, 99% yield).
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-5b6aa886f8694c6fb452d41c7298792d |
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| Source note | uspto-grants-2015_11 |
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