HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180014Generated: November 1, 2026
4-(Bromoacetyl)benzonitrile → HCID 54549064, compound
https://huagongshe.com/reaction/2180014
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(Bromoacetyl)benzonitrile | HCID 98654 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 53914229 | HCID 53914229 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 54549064 | HCID 54549064 | 35% |
Reaction Steps
4-Cyanophenacyl bromide (225 mg; 1 mmol) was added to a stirred solution of iso-propyl 3,7-diazabicyclo[3.3.1]nonane-3-carboxylate (from step (iv) above; 212 mg; 1 mmol) in MeCN (2 mL). After stirring for 15 min at 0° C., NaBH4 (40 mg; 1 mmol) was added, and the reaction was allowed to warm to rt over 45 minutes. The reaction mixture was concentrated, dissolved in CH2Cl2 and washed with NaHCO3 (aq.) and brine. The organic layer was separated, dried and concentrated to give an oil which was purified using column chromatography (hexane:EtOAc:IPA; 50:49:1) to give the sub-title compound in 35% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06887881B1 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-30dc8061ee13496faa248a3e549ea0b0 |
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| Source note | uspto-grants-2005_05 |
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