HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505917Generated: November 2, 2026
Formaldehyde → 4-(3-Bromophenyl)-1-methylpiperidine
https://huagongshe.com/reaction/1505917
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | tert-Butyl 4-(3-bromophenyl)piperidine-1-carboxylate | HCID 40425223 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | 4-(3-Bromophenyl)-1-methylpiperidine | HCID 53407842 | 99.3% |
Reaction Steps
A mixture of 4-(3-bromophenyl)-1-N-Boc piperidine (430 mg, 1.26 mmol), formic acid (5 mL) and formaldehyde (0.5 mL) was heated under microwave irradiation at 150° C. for 10 minutes. The cooled reaction mixture was loaded onto a 70 g SCX-2 cartridge which was washed with methanol (200 mL) and then eluted with 2N ammonia in methanol (200 mL). Concentration of the combined basic fractions in vacuo afforded the title compound (318 mg, 99%) as a brown oil. 1H NMR (CDCl3, 300 MHz): 7.38-7.36 (m, 1H); 7.35-7.29 (m, 1H); 7.17-7.14 (m, 2H); 3.03-2.92 (m, 2H); 2.52-2.37 (m, 1H); 2.32 (s, 3H); 2.10-1.99 (m, 2H); 1.87-1.69 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09216980B2 |
|---|
| Source dataset | uspto-grants-2015_12 |
|---|
| ORD ID | ord-861815beb0eb48c7bd5abe29508ab513 |
|---|
| Source note | uspto-grants-2015_12 |
|---|