HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-Dodecyl-5-methylisoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-(Bromomethyl)-3-dodecylisoxazole | HCID 10544376 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 3-Dodecyl-5-methylisoxazole | HCID 10491386 | — |
Reaction Steps
A suspension of 5-(bromomethyl)-3-dodecylisoxazole (9.99 g, 0.0302 mol) in dimethylsulfoxide (100 mL) was warmed to give a cloudy solution and allowed to cool. When the temperature reached +35° C., sodium borohydride (1.2 g, 0.032 mol) was added in one portion, and the mixture was stirred for 3 days under nitrogen at room temperature. The mixture was poured into 0.1M HCl (900 mL) and extracted with ether. The organic layer was washed (saturated NaCl), dried (MgSO4), and rotoevaporated. The residue was chromatographed on silica gel (160 g, 70-230 mesh) using petroleum ether-acetone (29:1, 10×200 mL) as eluent. Fraction 6 was rotoevaporated and dried in vacuo to give a white solid; yield 3.96 g (52%); mp 35°-38° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05441975 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-396152cb9e7d4a2fb101c1c293cc6e6c |
| Source note | uspto-grants-1995_08 |