HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Amino-1,5-naphthalenedisulfonic acid → 3-Hydroxy-2-methylbenzoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Amino-1,5-naphthalenedisulfonic acid | HCID 8563 | — |
| Reactant | (3-(Chlorocarbonyl)-2-methylphenyl)acetate | HCID 7010345 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Hydroxy-2-methylbenzoic Acid | HCID 252023 | — |
Reaction Steps
A process for the preparation of 3-acetoxy-2-methylbenzoyl chloride, which comprises reacting an alkali metal salt of 3-aminonaphthalene-1,5-disulfonic acid with alkali metal hydroxide and water in the weight ratio 1:(1 to 1.6):(1 to 1.6) at 220 to 320° C. to give the dialkali metal salt of 3-hydroxy-2-methylbenzoic acid, separating off insoluble constituents from the reaction mixture, then adjusting the reaction mixture to a pH of 11.5 to 1:3.5 by addition of acid and reacting it with acetic anhydride at -5 to 25° C., precipitating the 3-acetoxy-2-methylbenzoic acid by addition of acid, separating off the 3-acetoxy-2-methylbenzoic acid and reacting it with an inorganic acid chloride to give 3-acetoxy-2-methylbenzoyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06051732 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-bcf0ad5d15db4934a2b0602b8b87c9e1 |
| Source note | uspto-grants-2000_04 |