HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-dihydro-2H-pyran → 1-Chloro-4-(2-tetrahydropyranyloxy)nonane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Chlorononan-4-ol | HCID 20386082 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Product | 1-Chloro-4-(2-tetrahydropyranyloxy)nonane | HCID 20327686 | — |
Reaction Steps
To a stirred solution of 1-chloro-4-hydroxynonane (Example A, Step 2) (11.0 g., 0.062 mole) and dihydropyrane (5.2 g., 0.062 mole) cooled in an ice bath is added 5 drops of hydrochloric acid (conc.). A slight exothermic reaction is noted and when this is complete the reaction is allowed to come to room temperature, then stand for 2 hours. At the end of this period several pellets of sodium hydroxide are added and the reaction is distilled in vacuo. The yield of 1-chloro-4-(2-tetrahydropyranyloxy)nonane is 12.5 g. (77%), boiling 96°-102°/0.1 mm. Upon redistillation a boiling point of 90°-92°/0.1 mm. is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04091107 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-63d8953766aa4f0cbfe1a08ea1c5c844 |
| Source note | uspto-grants-1978_05 |