HuagongsheHuagongshe Chemistry Print Report · For research reference only
M-Cresol → 8-Methyl-1,2,3,4-tetrahydro-chromeno[3,4-c]pyridin-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | M-Cresol | HCID 342 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Methyl 4-oxopiperidine-3-carboxylate hydrochloride | HCID 2724028 | — |
| Product | 8-Methyl-1,2,3,4-tetrahydro-chromeno[3,4-c]pyridin-5-one | HCID 10608708 | 20.9% |
Reaction Conditions
| Temperature | 5 °C |
|---|
Reaction Steps
An 80% sulfuric acid solution (80 ml) is stirred and cooled to 5° C. in an ice bath and 3-methylphenol (10.8 ml, 0.10 moles) is added, followed by methyl-4-oxo-3-piperidine carboxylate hydrochloride (20.0 g, 0.10 moles). The mixture is allowed to warm gradually to room temperature. After 48 hours the solution is poured into ice water (400 ml) and stirred until a crystalline precipitate forms. Concentrated ammonium hydroxide is added until the mixture is strongly basic. After one hour the precipitate is filtered off, rinsed with concentrated ammonium hydroxide, then water, and dried. Recrystallization from acetonitrile gave the product (4.5 g), mp 128°-130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04382939 |
| Source dataset | uspto-grants-1983_05 |
| ORD ID | ord-4f3f6a0967c5498992cec6b0d1d23097 |
| Source note | uspto-grants-1983_05 |