HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267901Generated: October 30, 2026
Benzyl Chloride → 4,5-Dihydro-4-methyl-2-phenyl-4-[(phenylmethoxy)methyl]oxazole
https://huagongshe.com/reaction/267901
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (4-Methyl-2-phenyl-4,5-dihydro-1,3-oxazol-4-yl)methanol | HCID 226853 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4,5-Dihydro-4-methyl-2-phenyl-4-[(phenylmethoxy)methyl]oxazole | HCID 21552761 | — |
Reaction Steps
A suspension of 4-hydroxymethyl-4-methyl-2-phenyloxazoline (19.1 grams, prepared by the method described in J. Amer, Chem. Soc. 1945, 67, 1069) in toluene (200 milliliters) was added slowly to a stirred suspension of sodium hydride (2.4 grams) in toluene (50 milliliters). Some warming was necessary to initiate the reaction. The mixture was then heated under reflux for 2 hours with stirring. Benzyl chloride (13.0 grams) was added to the mixture over a period of 10 minutes. The mixture was heated under reflux for a further 5 hours and then allowed to stand at room temperature for 16 hours. The mixture was washed with water (3 × 200 milliliters), dried (MgSO4) and evaporated under reduced pressure. The residue was distilled in vacuo to give the desired product, boiling point 147°-149°C at 0.3 Torr.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03945998 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-62fcc27052124492be4366b777cf5817 |
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| Source note | uspto-grants-1976_03 |
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