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HRID 8079作成日:2026年10月24日

Hydrochloric Acid → HCID 178418889、化合物

https://huagongshe.com/ja/reaction/8079

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Dimethyl oxalateHCID 11120—
反応物1-(4-(Methylthio)phenyl)ethan-1-oneHCID 74501—
反応物Sodium MethoxideHCID 10942334—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
溶媒HexaneHCID 8058—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 178418889HCID 17841888979%

反応条件

温度0 °C

反応手順

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 drop-wise over 15 minutes 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 solid 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% yield) 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+). Anal. calcd. for C12H12O4S: C, 57.13; H, 4.79; S, 12.71. Found: C, 56.85; H, 4.76; S, 12.43.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087630B2
出典データセットuspto-grants-2006_08
ORD IDord-f742f3db871b4af2af5afa3faa6671a2
出典メモuspto-grants-2006_08