HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Difluorobenzoic acid → 1-(3,4-Difluorophenyl)ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Difluorobenzoic acid | HCID 99166 | — |
| Reactant | 4,5-Difluoro-2-nitrobenzoic acid | HCID 4219630 | — |
| Product | 1-(3,4-Difluorophenyl)ethan-1-one | HCID 123052 | — |
Reaction Steps
Briefly, the benzoyl ester derivatives of formula II are prepared by reacting 5-fluoro-4-halo-2-nitrobenzoic acid with a chlorinating agent, such as thionyl chloride or trichlorophosphorous, followed by reacting the acid chloride so formed with a dialkylmalonate. The 4,5-difluoro-2-nitrobenzoic acid starting material can be prepared by nitration in mixed acid of 3,4-difluorobenzoic acid, which is obtained by oxidation 3,4-difluoroacetophenone. The 4- chloro-5-fluoro-2-nitrobenzoic acid starting material can be obtained by the following process:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05138088 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-e410c75b2d4843988731bcdd374b5e1d |
| Source note | uspto-grants-1992_08 |