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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113738Generated: October 26, 2026

Hydrochloric Acid → HCID 178418889, compound

https://huagongshe.com/reaction/2113738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethyl oxalateHCID 11120—
Reactant1-(4-(Methylthio)phenyl)ethan-1-oneHCID 74501—
ReactantSodium MethoxideHCID 10942334—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 178418889HCID 17841888979%

Reaction Conditions

Temperature0 °C

Reaction Steps

Dimethyloxalate (26 g, 180.7 mmol) was added to a stirred suspension of sodium methoxide (9.75 g, 180.7 mmol) in dry toluene (200 mL) at 0° C. The white suspension was stirred for 15 min at 0° C. A solution of 4′-(methylthio)acetophenone (15 g, 90.4 mmol) in dry toluene (150 mL) was then added dropwise over 15 min giving a yellow suspension which was stirred for 2 hours at room temperature. The thick yellow suspension was transferred to a 2 liter flask and stirred vigorously with 10% HCl (250 mL) and EtOAc (200 mL) to dissolve all the solids present. The organic layer was separated and the aqueous layer was extracted with EtOAc (100 mL). The combined organic extracts were washed with water (250 mL), dried over Na2SO4 and the solvent was evaporated under reduced pressure to give thick brown oil. The brown oil was dissolved in CH2Cl2 (25 mL) and hexane (125 mL) and left in a freezer at −20° C. for 16 hours to give the title compound (18 g, 79%) as orange color solid. mp 81° C. 1H-NMR (300 MHz, CDCl3) δ 7.83 (d, J=8.6 Hz, 2H), 7.23 (d, J=8.6 Hz, 2H), 6.97 (s, 1H), 3.89 (s, 3H), 2.47 (s, 3H); 13C-NMR (75 MHz, CDCl3); mass spectrum (API-TIS) m/z 253 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432285B2
Source datasetuspto-grants-2008_10
ORD IDord-d867f62dfa85473d8ae6ff97fb4c2125
Source noteuspto-grants-2008_10