HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2,5-dibromopentanoate → Methyl 5-bromo-2-(5-ethoxycarbonyl-2-nitrophenoxy)valerate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2,5-dibromopentanoate | HCID 10912698 | — |
| Reactant | Ethyl 3-hydroxy-4-nitrobenzoate | HCID 12784564 | — |
| Product | Methyl 5-bromo-2-(5-ethoxycarbonyl-2-nitrophenoxy)valerate | HCID 21282570 | — |
Reaction Steps
By a process similar to that of Reference Example 5, ethyl 3-hydroxy-4-nitrobenzoate was allowed to react with methyl 2,5-dibromovalerate to give methyl 5-bromo-2-(5-ethoxycarbonyl-2-nitrophenoxy)valerate as an oily product (yield: 80.2%). This product was subjected to catalytic reduction to obtain ethyl 2-(3-bromopropyl)-3,4-dihydro-3-oxo-2H-1,4-benzoxazine-7-carboxylate, m.p. 118°-119° C. The yield was 90.7%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04789675 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-9561cb3d8cf341caa58fde33fdac3c70 |
| Source note | uspto-grants-1988_12 |