HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-dihydro-2H-pyran → HCID 18391989, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)- | HCID 18462 | — |
| Reactant | (R)-(+)-1-Benzyl-3-pyrrolidinol | HCID 643472 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18391989 | HCID 18391989 | 120% |
Reaction Steps
To a stirred solution of (R)-(+)-1-benzyl-3-pyrrolidinol (5.00 g, 28 mmol) and D-camphor-10-sulfonic acid (6.97 g, 30 mmol) in CH2Cl2 (10 ml) was added 3,4-dihydro-2H-pyran (20 ml) at rt and the reaction mixture was stirred for 14 h (in most cases, the reaction was completed after exothermic reaction subsided). The reaction mixture was diluted with CH2Cl2 (100 ml), washed with saturated NaHCO3 aqueous solution, dried (Na2SO4), and concentrated to give brown oil. This tas purified by column chromatography (silica gel:200 g, CH2Cl2 /MeOH:40/1 as eluent) to give 8.78 g (97.6%) of desired compound as brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05952369 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-78637cfff7644dd982b9f85acf4d6edf |
| Source note | uspto-grants-1999_09 |