HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 357800, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | Ethyl 6-hydroxyhexanoate | HCID 357781 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 357800 | HCID 357800 | — |
Reaction Steps
66 g. (0.412 mol) of ethyl 6-hydroxyhexanoate [prepared as described by S. R. Sandler and W. Karo, in `Organic Functional Group Preparation` , Academic Press, New York, and London, vol. 1, page 262. (cf. G. B. Hatch and H. Adkins, J. Am. Chem. Soc., 59 1694 (1937))] were dissolved in 400 ml. of methylene chloride, and the mixture was reacted with 45 g. of dihydropyran and 1 g. of p-toluenesulphonic acid at 25°C. for 20 minutes. The reaction mixture was washed with an aqueous sodium bicarbonate solution, dried and concentrated. The residue was distilled in vacuo to obtain 77 g. of the title compound having the following physical characteristics:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03978229 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-0f7632a4a0e54e04b08429a5f769b3db |
| Source note | uspto-grants-1976_08 |