Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 3-(Bromomethyl)-4-nitrobenzoic acid | HCID 20493671 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 89739572 | HCID 89739572 | 87% |
Reaction Steps
An aqueous solution of 25% w/v ammonia (100 mL) was treated with EtOH (200 mL) and cooled to −78° C. The mixture was slowly treated with a cooled (−78° C.) solution of the benzylbromide (2.58 g, 10.0 mmol) in ethanol (100 mL). The mixture was then allowed to come to room temperature and stirred for 48 h. The mixtures were evaporated under reduced pressure and the residue solid was washed with CH2Cl2 to afford 3-(aminomethyl)-4-nitrobenzoic acid (1.7 g, 87% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284299B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-2c799aa0333a4e54a15f7bc6b8881051 |
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| Source note | uspto-grants-2016_03 |
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