HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → Benzyl tetrahydro-2H-pyran-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Oxane-4-carboxylic acid | HCID 219302 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzyl tetrahydro-2H-pyran-4-carboxylate | HCID 23131611 | 70.1% |
Reaction Conditions
| Temperature | 60 °C |
|---|
Reaction Steps
A mixture of tetrahydropyran-4-yl-carboxylic acid (910 mg, 6.99 mmol) and SOCl2 (5.0 mL) was stirred for 1 h at 60° C. and concentrated in vacuo. To the residue were added benzyl alcohol (1.52 g, 14.1 mmol) and tetrahydrofuran (5.0 mL) at ambient temperature. The resulting mixture was stirred for 13 h at ambient temperature and concentrated in vacuo. The residue was purified by preparative thin layer chromatography (silica gel, eluting with hexane/ethyl acetate (2:1)) to give 1.08 g (70%) of the title compound as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07737163B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-8fd06a8b3539453b86ef5bd3c688a452 |
| Source note | uspto-grants-2010_06 |