HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412708Generated: October 28, 2026
Trichloroacetyl isocyanate → 2-Methoxyimino-2-(3-carbamoyloxyphenyl)acetic acid
https://huagongshe.com/reaction/2412708
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trichloroacetyl isocyanate | HCID 76400 | — |
| Reactant | 2-Methoxyimino-2-(3-hydroxyphenyl)acetic acid | HCID 54390551 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Methoxyimino-2-(3-carbamoyloxyphenyl)acetic acid | HCID 54345149 | — |
Reaction Steps
Trichloroacetyl isocyanate (70 ml) was dropwise added over 6 minutes at ambient temperature to a solution of 2-methoxyimino-2-(3-hydroxyphenyl)acetic acid (syn isomer) (40 g) in dry dioxane (200 ml), and the resulting mixture was stirred for 5 hours at ambient temperature. Dioxane was distilled off and to the residue were added ethyl acetate (200 ml) and by small portions water (200 ml) under ice-cooling. The mixture containing trichloroacetylcarbamoyl 2-methoxyimino-2-(3-trichloroacetylcarbamoyloxyphenyl)acetate was stirred for 5 hours at ambient temperature keeping the pH value of the mixture at 6.0 to 6.4 by adding an aqueous solution of sodium bicarbonate. The resulting mixture was wahsed twice with ethyl acetate. The aqueous layer was adjusted to pH2 with a 10% hydrochloric acid and extracted three times with ethyl acetate. The combined ethyl acetate extracts were washed twice with an aqueous solution of sodium chloride and dried over magnesium sulfate. The solvent was distilled off and precipitating crystals were collected by filtration to give colorless crystals of 2-methoxyimino-2-(3-carbamoyloxyphenyl)acetic acid (syn isomer) (15 g), mp 163° C. (dec.). The same compound (5.4 g) was obtained from the mother liquor.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04493833 |
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| Source dataset | uspto-grants-1985_01 |
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| ORD ID | ord-34339335564f48cc9721fa426845f2cb |
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| Source note | uspto-grants-1985_01 |
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