HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-(1-methylethyl)-(2-nitro-6-fluorophenyl)methylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Fluoro-6-nitrobenzaldehyde | HCID 13524043 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(1-methylethyl)-(2-nitro-6-fluorophenyl)methylamine | HCID 17777165 | — |
Reaction Steps
To a solution of 2-nitro-6-fluorobenzaldehyde(1.21 g, 7.16 mmol) in dry methanol (15 ml), was added isopropyl amine (1 ml, 11.4 mmol) and the mixture stirred for 24 hours at room temperature in argon atmosphere. Then NaBH4 (0.3 g, 7.9 mmol) was added and the reaction mixture was stirred for 36 hours. The suspension was neutralized by addition of HCl 5N, then was extracted with diethyl ether (1×100 ml) and dried over MgSO4 and evaporated at reduced pressure to afford N-(1-methylethyl)-(2-nitro-6-fluorophenyl)methylamine as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05929072 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-37b2d576b5c846d6b94415104c849d74 |
| Source note | uspto-grants-1999_07 |