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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1518014Generated: November 1, 2026

Triethylamine → HCID 21873648, compound

https://huagongshe.com/reaction/1518014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl ThioglycolateHCID 12185—
ReactantEthyl 2,4-difluoro-5-nitrobenzoateHCID 22330120—
ReactantEthyl 4-[(2-ethoxy-2-oxoethyl)thio]-2-fluoro-5-nitrobenzoateHCID 59560604—
SolventDichloromethaneHCID 6344—
ProductHCID 21873648HCID 2187364896%

Reaction Steps

4-Ethoxycarbonylmethylsulfanyl-2-fluoro-5-nitro-benzoic acid ethyl ester. To a solution of 2,4-difluoro-5-nitro-benzoic acid ethyl ester (7.0 g, 0.030 mol) in CH2Cl2 (125 mL) was added Et3N (5.0 mL, 36 mmol) at 0° C. Following the addition of ethyl 2-mercaptoacetate (3.30 mL, 30.3 mmol), the solution was warmed to RT and stirred for 18 h. The reaction mixture was partitioned between H2O and CH2Cl2 (400 mL). The organic layer was washed with 0.05 M HCl (200 mL), brine (200 mL), dried (MgSO4), filtered and concentrated to provide 9.6 g (96%) of the title compound as a tan solid. MS (ESI): exact mass calculated for C13H14FNO6S, 331.05; m/z not found. 1H NMR (500 MHz, CDCl3): 8.88 (d, J=6.9, 1H), 7.14 (d, J=11.4, 1H), 4.41 (q, J=7.2, 2H), 4.29 (q, J=7.2, 2H), 3.75 (s, 2H), 1.40 (t, J=7.2, 3H), 1.29 (t, J=7.2, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232391B2
Source datasetuspto-grants-2012_07
ORD IDord-38674fad47e841ddaf83728a0fc75ce4
Source noteuspto-grants-2012_07