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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1819971Generated: October 30, 2026

Ethyl Thioglycolate → HCID 57890097, compound

https://huagongshe.com/reaction/1819971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl ThioglycolateHCID 12185—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 57890216HCID 57890216—
SolventEthanolHCID 702—
ProductHCID 57890097HCID 5789009727%

Reaction Steps

To a solution of 2.68 M sodium ethoxide (507 μl, 1.36 mmol) in EtOH (2 ml) is added ethyl 2-mercaptoacetate (149 μl, 1.36 mmol) and stirred at RT for 30 m. The mixture is added a solution of toluene-4-sulfonic acid 5-{1-[4-(tert-butyl-dimethyl-silanyloxy)-3-methyl-phenyl]-1-ethyl-propyl}-3-methyl-thiophen-2-ylmethyl ester (740 mg, 1.29 mmol) in EtOH (2 ml) is added and refluxed for 15 m. The reaction is concentrated and partitioned between EtOAc (100 ml) and 0.2N HCl (50 ml). The organic layer is washed with water (50 ml), dried (MgSO4), concentrated, and chromatographed (12 g SiO2, 5% EtOAc/Hex) to yield the title compound (180 mg, 27%). 1NMR (400 MHz, CDCl3) δ 7.00 (d, 1H, J=2.2 Hz), 6.92 (dd, 1H, J=8.4, 2.2 Hz), 6.64 (d, 1H, J=8.4 Hz), 6.46 (s, 1H), 4.17 (q, 2H, J=7.2 Hz), 3.92 (s, 2H), 3.14 (s, 2H), 2.16 (s, 3H), 2.12 (s, 3H), 2.07-1.98 (m, 4H), 1.28 (t, 3H, J=7.0 Hz), 1.00 (s, 9H), 0.68 (t, 6H, J=7.3 Hz), 0.20 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601850B2
Source datasetuspto-grants-2009_10
ORD IDord-4429805bc6d5408b815e54919818f6ea
Source noteuspto-grants-2009_10