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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503640Generated: October 30, 2026

Ethyl Thioglycolate → HCID 60631860, compound

https://huagongshe.com/reaction/1503640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl ThioglycolateHCID 12185—
ReactantSodium hydrideHCID 24758—
Reactant4-Fluoro-3-nitrobenzaldehydeHCID 598129—
SolventDimethylformamideHCID 6228—
ProductHCID 60631860HCID 6063186024.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of ethyl-2-mercaptoacetate (0.7 mmol) in dry DMF (2.5 ml), sodium hydride (0.85 mmol) was added 0° C. After 15 minutes, 4-fluoro-3-nitrobenzaldehyde (0.7 mmol) was added and the mixture was heated at 60° C. overnight and monitored by TLC until completion. After cooling, the solvent was removed under reduced pressure. The residue was chromatogaphed on a silica gel column (cyclogexane/ethyl acetate 4/1 as eluent) to give 46 mg of ethyl 2-(4-formyl-2-nitrophenylthio)acetate as yellow compound (yield 24%). 1H NMR, (250 MHz, CDCl3): δ 1.25 (t, J=7.5 Hz, 3H), 3.80 (s, 2H), 4.21 (q, J=7.75, 2H), 7.64 (d, J=9.75, 1H), 8.03 (d, J=9.75, 1H), 8.68 (s, 1H), 10.00 (s, 1H) 13C NMR (126 MHz, CDCl3): δ 15.4, 36.5, 63.8, 128.5, 129.3, 133.9, 145.6, 147.1, 169.5, 190.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212196B2
Source datasetuspto-grants-2015_12
ORD IDord-915bdae046d14a7abd8ee1720df454c7
Source noteuspto-grants-2015_12