HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707168Generated: October 26, 2026
2-Thiopheneglyoxylic acid → 2-Hydroxyimino(thien-2-yl)acetic acid
https://huagongshe.com/reaction/1707168
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Thiopheneglyoxylic acid | HCID 77694 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Hydroxyimino(thien-2-yl)acetic acid | HCID 73629644 | 51% |
Reaction Steps
A cooled solution of hydroxylamine hydrochloride (0.884 g) and sodium bicarbonate (1.08 g) in water (20 ml.) was added to a cooled (0°) solution of thien-2-yl-glyoxylic acid (2.0 g) and sodium bicarbonate (1.08 g) in water (20 ml.). After two days at 20° the solution was extracted with ether, cooled and acidified with concentrated hydrochloric acid. The resulting white solid was filtered off (0.564 g) and the filtrate was then thoroughly extracted with ether. The combined extracts were washed with brine, dried and concentrated. The solid residue was triturated with benzene to give the oxime (syn-isomer) (1.05 g; 51%), m.p. 132°, λmax. (ethanol) 284 nm (ε 9,500), λmax. (Nujol) 2590 and 1706 (CO2H) and 1655 cm-1 (C=N), τ (DMSO-d6), -2.5 to -0.5 (broad multiplet; N--OH and COOH), 2.36 (multiplet; thienyl C-5 H) and 2.82 (multiplet; thienyl C-3 H and C-4 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04209616 |
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| Source dataset | uspto-grants-1980_06 |
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| ORD ID | ord-4f4be94a626e4402a3d47f22384adabd |
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| Source note | uspto-grants-1980_06 |
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