HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463840Generated: October 29, 2026
Sodium Methoxide → 2-t-Butoxycarbonylmethoxyimino-2-(3-chloro-4-hydroxyphenyl)acetic acid
https://huagongshe.com/reaction/463840
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | tert-Butyl (aminooxy)acetate | HCID 12919121 | — |
| Reactant | 2-(3-Chloro-4-hydroxyphenyl)-2-oxoacetic acid | HCID 12961139 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-t-Butoxycarbonylmethoxyimino-2-(3-chloro-4-hydroxyphenyl)acetic acid | HCID 136149112 | 79.1% |
Reaction Steps
A mixture of 2-(3-chloro-4-hydroxyphenyl)glyoxylic acid (2.0 g.), O-t-butoxycarbonylmethylhydroxylamine (1.62 g.) and methanol (20 ml.) was adjusted to pH 5 to 6 by adding an 1N methanol solution of sodium methoxide and stirred for 3 hours at ambient temperature. The reaction mixture was concentrated to dryness under reduced pressure and the residue was dissolved in an 1N aqueous solution of sodium hydroxide to adjust to pH 7.0. The aqueous solution was washed with ether, adjusted to pH 2.0 with 10% hydrochloric acid under ice-cooling and extracted with ether. The extract was washed with water and dried over magnesium sulfate. The solution was concentrated to dryness under reduced pressure to give crystals of 2-t-butoxycarbonylmethoxyimino-2-(3-chloro-4-hydroxyphenyl)acetic acid (syn isomer) (2.6 g.), mp 116° to 118° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04544653 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-2e74ef3c846a4494aac5618916fa4ebe |
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| Source note | uspto-grants-1985_10 |
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