HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxetane → 2,6,7-Trioxabicyclo(2.2.2)octane, 4-cyclohexyl-1-(4-ethylnylphenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxetane | HCID 10423 | — |
| Reactant | 4-(1,2-dibromoethyl)benzoyl Chloride | HCID 184002 | — |
| Reactant | (3-Cyclohexyloxetan-3-yl)methanol | HCID 19373305 | — |
| Product | 2,6,7-Trioxabicyclo(2.2.2)octane, 4-cyclohexyl-1-(4-ethylnylphenyl)- | HCID 176087 | — |
Reaction Steps
Utilizing Procedure 2, 4-cyclohexyl-1-(4-ethynylphenyl)-2,6,7-trioxabicyclo[2.2.2]octane was prepared from its respective oxetane. The 3-cyclohexyl-3-hydroxymethyloxetane was reacted with 4-(1,2-dibromoethyl)benzoyl chloride by the method of Procedure 2. The resulting product was characterized by NMR (300 MHz, CDCl3): δ 1.0-1.4 and 1.6-2.0 (11H, m, cyclohexyl CH2), 3.9-4.1 (2H, m, CH2Br), 4.4 (2H, s, CH2O), 4.55 (4H, d of d, CH2OCH2), 5.1 (1H, d of d, ArCHBr), 7.45 (2H, d, aromatic), 8.1 (2H, d, aromatic).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04772624 |
| Source dataset | uspto-grants-1988_09 |
| ORD ID | ord-36eba9e7210646b4bc38ca3444cc9dec |
| Source note | uspto-grants-1988_09 |