HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358082Generated: October 30, 2026
Sodium Hydroxide → 2-Tert-butoxycarbonylmethoxyimino-2-(1,2,5-thiadiazol-3-yl)acetic acid
https://huagongshe.com/reaction/358082
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (1,2,5-Thiadiazol-3-yl)glyoxylic acid | HCID 12906559 | — |
| Reactant | tert-Butyl (aminooxy)acetate | HCID 12919121 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Tert-butoxycarbonylmethoxyimino-2-(1,2,5-thiadiazol-3-yl)acetic acid | HCID 53743269 | 91.9% |
Reaction Steps
To a solution of (1,2,5-thiadiazol-3-yl)glyoxylic acid (6 g) in tetrahydrofuran (30 ml) and water (30 ml) was added tert-butoxycarbonylmethoxyamine (8.37 g) at ambient temperature. The mixture was adjusted to pH 4.5-5.0 with 4N aqueous sodium hydroxide and stirred at ambient temperature for 4 hours. The mixture was adjusted to pH 7.5 with 4N aqueous sodium hydroxide and washed with ethyl acetate (100 ml×2). The aqueous solution was acidified to pH 2.0 with 10% hydrochloric acid and extracted with ethyl acetate (100 ml×2). The organic layer was washed with an aqueous sodium chloride and dried over magnesium sulfate. The solution was evaporated in vacuo to give 2-tert-butoxycarbonylmethoxyimino-2-(1,2,5-thiadiazol-3-yl)acetic acid (syn and anti mixture) (10.02 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04464369 |
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| Source dataset | uspto-grants-1984_08 |
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| ORD ID | ord-df38488b7e454b3bb34fad0e4d1dffcb |
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| Source note | uspto-grants-1984_08 |
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