HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyl orthoformate → 4,4-Dimethoxypiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | Piperonylamine | HCID 2723901 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4,4-Dimethoxypiperidine | HCID 557469 | — |
Reaction Steps
Into 9 ml of methanol were dissolved 0.69 g of 4-piperidone hydrochloride monohydrate, 0.74 ml of trimethyl orthoformate and 86 mg of p-toluenesulfonic acid monohydrate, and the reaction was conducted at room temperature for 24 hours. The reaction mixture was evaporated under reduced pressure to remove the solvent. The residue was dissolved into 2 ml of N,N-dimethylacetamide and admixed with 1.4 ml of triethylamine to give a solution of 4,4-dimethoxypiperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05981522 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-a9f177263f9d43879d3ff0225fa863ad |
| Source note | uspto-grants-1999_11 |