HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719490Generated: October 30, 2026
Toluene → tert-Butyl 4-((methylamino)methyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/719490
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Tert-butyl 4-(methylcarbamoyl)piperidine-1-carboxylate | HCID 2757240 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl 4-((methylamino)methyl)piperidine-1-carboxylate | HCID 21934652 | 60.2% |
Reaction Steps
In a 32 mL reaction vial was placed a stir bar and 4-methylcarbamoyl-piperidine-1-carboxylic acid tert-butyl ester (0.97 g) dissolved in 12.8 mL anhydrous THF. The solution was cooled to 0° C. with an ice-bath. A 65% toluene solution of Red-A1 (3.66 mL) was added dropwise at 0° C. After the addition was completed, the mixture was stirred under N2 at room temperature until all the starting materials were just consumed. The reaction mixture was worked up with H2O at 0° C., extracted with EtOAc (×3). The EtOAc extract was washed with saturated NaCl solution. After drying over Na2SO4, the organic layer was concentrated to give 550 mg of crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07132426B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-8725da3069ac42508ee873142c413530 |
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| Source note | uspto-grants-2006_11 |
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