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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381244Generated: October 30, 2026

Methyl Thioglycolate → Methyl 3-amino-5-(3-chlorophenyl)thiophene-2-carboxylate

https://huagongshe.com/reaction/381244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl ThioglycolateHCID 16907—
ReactantSodium MethoxideHCID 10942334—
Reactant3-Chloro-3-(3-chlorophenyl)-2-propenenitrileHCID 53758661—
SolventMethanolHCID 887—
ProductMethyl 3-amino-5-(3-chlorophenyl)thiophene-2-carboxylateHCID 11994772—

Reaction Steps

Sodium pellets were slowly added to methanol solution to form NaOMe in situ, then methyl thioglycolate was added over a period of 20 minutes to the methanol solution. A solution of 3-Chloro-3-(3-chloro-phenyl)-acrylonitrile in methanol was added slowly and was brought to reflux for 1 hour. The reaction mixture was cooled to room temperature and methanol was concentrated to 100 mL and 200 mL of water was added, stirred for 30 minutes and the yellow precipitate was collected and washed with water several times to yield a yellow crystalline compound, mp 92-95° C. 1H NMR (DMSO-d6) δ1.60 (s, 6H), 7.30 (d, 1H, J=8.41 Hz), 7.41(d, 1H, J=8.41 Hz), 10.47 (s, 1H); MS(+APCI)m/z 213(M+H); Anal. Calc. For C9H9ClN2O2: C, 50.84; H, 4.27; N, 13.17. Found: C, 50.99; H, 4.28; N, 12.98.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06306851B1
Source datasetuspto-grants-2001_10
ORD IDord-b92dca44009f4559a4acc43382ded976
Source noteuspto-grants-2001_10