HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Naphthoic acid → 4-Chloronaphthalene-1-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Naphthoic acid | HCID 6847 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | HCID 57234554 | HCID 57234554 | — |
| Product | 4-Chloronaphthalene-1-carboxylic acid | HCID 12749143 | — |
| Product | HCID 57234554 | HCID 57234554 | — |
Reaction Steps
A process for the preparation of 4-bromo-naphthalic acid anhydride by bromination of an alkali metal salt of naphthalic acid in an aqueous medium at a pH of 6.8 to 9 by dropwise adding 0.55 to 0.65 mol of bromine per mol of naphthalic acid and oxidizing the bromine at the same pH-value with chlorine. By this process 4-bromo-naphthalic acid anhydride can be obtained in a quantitative yield whereby the formation of 4-chloro-naphthalic acid is avoided.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03954810 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-3ebb7487147e441c9cc96a456a2fad81 |
| Source note | uspto-grants-1976_05 |