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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 385178생성일: 2026년 10월 26일

Hydrochloric Acid → 4-Isothiocyanato-2-chlorobenzoic acid

https://huagongshe.com/reaction/385178

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물IodineHCID 807—
반응물Carbon DisulfideHCID 6348—
반응물TriethylamineHCID 8471—
반응물4-Amino-2-chlorobenzoic acidHCID 17154—
반응물Sodium SulfiteHCID 24437—
반응물Sodium BicarbonateHCID 516892—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물4-Isothiocyanato-2-chlorobenzoic acidHCID 2273100662%

반응 단계

Carbon disulfide (0.26 mL, 4.4 mmol) was added to a mixture comprising 4-amino-2-chlorobenzoic acid (0.26 g, 1.5 mmol), tetrahydrofuran (1.0 mL), water (1.0 mL) and triethylamine (0.51 mL, 3.6 mmol), followed by stirring at room temperature for 24.5 hours. To the obtained reaction mixture, a tetrahydrofuran (1.0 mL) solution of iodine (0.41 g, 1.6 mmol) was dropwise added over a period of 5 minutes at 0° C., followed by stirring at 0° C. for further two hours. Thereafter, 1M hydrochloric acid (1.5 mL) and sodium sulfite (38 mg, 0.30 mmol) were added and stirred. Then, ethyl acetate (6 mL) was added, and the organic layer was separated and concentrated under reduced pressure to dryness. To the residue, water (4 mL) and sodium hydrogencarbonate (0.14 g, 1.7 mmol) were added, and the insoluble matter was removed by filtration. To the filtrate, 1M hydrochloric acid (1.5 mL) and water (2.0 mL) were added, and the precipitated solid was collected by filtration. To this solid, ethyl acetate (6 mL), water (2.0 mL) and sodium hydrogencarbonate (25 mg, 1.7 mmol) were added, and the organic layer was concentrated under reduced pressure to dryness to obtain 4-isothiocyanato-2-chlorobenzoic acid as a white solid (0.20 g, yield: 62%, HPLC purity: 91%, HPLC retention time: 3.9 min). LC-MS ES-212, 214 (retention time: 4.2 min, condition 1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367857B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-b03e4b7becd84cedbfd998405342dfd3
출처 메모uspto-grants-2013_02