HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 1-Tert-butyl-4-chloropiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 1-Methyl-3,4-dihydroisoquinoline | HCID 231502 | — |
| Reactant | HCID 18382671 | HCID 18382671 | — |
| Reactant | HCID 178418332 | HCID 178418332 | — |
| Product | 1-Tert-butyl-4-chloropiperidine | HCID 11423872 | — |
Reaction Steps
The imine bond can be activated by quaternization to allow the nucleophilic addition of Grignard reagent. Methyl iodide was added to 1-methyl-3,4-dihydroisoquinoline, generating the iminium salt 1,2-dimethyl-3,4-dihydroisoquinolinium iodide.20 This iminium salt is more reactive than the imine. Methylmagnesium chloride reacted with the iminium, generating 1,1,2-trimethyl-1,2,3,4-tetrahydroisoquinoline. The reaction of methylmagnesium chloride with the iminium salt N-isopropylidene-4-chloropiperidinium chloride gave 1-tert-butyl-4-chloropiperidine.21
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09440948B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-651143b2b3ac4b9082fb05b5c5ffe788 |
| Source note | uspto-grants-2016_09 |