HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370023Generated: October 25, 2026
Methanol → 4-Amino-3-chloro-5-methoxyiminomethylbenzoic acid
https://huagongshe.com/reaction/370023
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Amino-3-chloro-5-methoxyiminomethylbenzoate | HCID 73432822 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Amino-3-chloro-5-methoxyiminomethylbenzoic acid | HCID 54099134 | 94% |
Reaction Steps
In a 5-liter three-necked round-bottomed flask was placed 210 g (0.86 moles) of the previously prepared 4-amino-3-chloro-5-methoxyiminomethylbenzoate, 1.7 l of methanol and 462 g (1.73 moles) of 15% aqueous sodium hydroxide. The resulting mixture was refluxed for 3 hours, after which the reaction mixture was stirred overnight at room temperature. The reaction mixture was concentrated using a rotary evaporator. The crude reaction mixture was dissolved in 2 l of water. The resulting aqueous solution was washed once with 500 mL of ethyl acetate, cooled in an ice bath and acidified to pH=2 with concentrated hydrochloric acid. The expected 4-amino-3-chloro-5-methoxyiminomethylbenizoic acid precipitated as a light yellow solid which was separated by suction filtration. The filter cake was washed with a 1:2 mixture of ethyl ether and hexane yielding after drying 185.2 g (94% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06140362 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-5a8fb1205e6f4ed38e76203e7a0d99f6 |
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| Source note | uspto-grants-2000_10 |
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