HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-dihydro-2H-pyran → Methyl 3-(2-tetrahydropyranyloxy)cyclohexanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | Methyl 3-hydroxycyclohexane-1-carboxylate | HCID 12209242 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methyl 3-(2-tetrahydropyranyloxy)cyclohexanecarboxylate | HCID 13236238 | 65.8% |
Reaction Steps
To a solution of methyl 3-hydroxycyclohexanecarboxylate [J. Am. Chem. Soc., 70, 1898 (1948)] (61 g) in ether (500 ml), 2,3-dihydropyran (49 g) and p-toluenesulfonic acid monohydrate (1 g) were added. The mixture was stirred at room temperature for 6 hours and washed with water and dried (MgSO4). The ether was distilled off, and the oily residue was distilled under reduced pressure to give methyl 3-(2-tetrahydropyranyloxy)cyclohexanecarboxylate (61.5 g, 60.2%, b.p. 120°-123° C./0.3 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04461902 |
| Source dataset | uspto-grants-1984_07 |
| ORD ID | ord-cd85fc058c144124b41814cf05302224 |
| Source note | uspto-grants-1984_07 |