HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dioxane → HCID 67617352, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 67617268 | HCID 67617268 | — |
| Product | HCID 67617352 | HCID 67617352 | — |
Reaction Steps
In a similar manner to the process for precursor δ), 9.6 g of methyl 2-[2-(acetyl-2,5-dimethylphenoxymethyl)phenyl]E-but-2-enoate in 60 ml of dioxane were reacted to give the carboxylic acid. After concentrating on a rotary evaporator a yellow oil remained which in addition to 70% of the title compound contained a further 30% of the diacid formed by hydrolysis of the methyl butanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05545664 |
| Source dataset | uspto-grants-1996_08 |
| ORD ID | ord-6ca1870ae7de490b9a95d3d2446f33fc |
| Source note | uspto-grants-1996_08 |