Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,3-Dioxan-5-ol, 2-phenyl- | HCID 74362 | — |
| Reactant | 2-(Chloromethyl)anisole | HCID 81495 | — |
| Product | HCID 20364891 | HCID 20364891 | 77.9% |
Reaction Steps
5-Hydroxy-2-phenyl-1,3-dioxane (8.4 g, 0.05 mole) was reacted with sodium hydride and 2-methoxybenzyl chloride (7.8 g, 0.05 mol) according to the method of Example 2, except that the mixture was heated at 100° C for 12 hours, to give 11.7 g of yellow oil. The oil was distilled under 1 × 10-5 mm to give 4.6 g of product, which distilled at a pot temperature of 180°-190° C. VPC analysis of the product showed it to contain 72% cis-5-(2methoxybenzyloxy)-2-phenyl-1,3-dioxane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04077982 |
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| Source dataset | uspto-grants-1978_03 |
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| ORD ID | ord-25cedd1febbd46dda444e9faa737ecbd |
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| Source note | uspto-grants-1978_03 |
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