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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiopheneglyoxylic acidHCID 77694—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
Product2-Hydroxyimino(thien-2-yl)acetic acidHCID 7362964451%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04209616
Source datasetuspto-grants-1980_06
ORD IDord-4f4be94a626e4402a3d47f22384adabd
Source noteuspto-grants-1980_06