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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 385183생성일: 2026년 10월 24일

Hydrochloric Acid → 3-Isothiocyanato-4-methoxybenzoic acid

https://huagongshe.com/ko/reaction/385183

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물IodineHCID 807—
반응물Carbon DisulfideHCID 6348—
반응물TriethylamineHCID 8471—
반응물3-Amino-4-methoxybenzoic acidHCID 17823—
반응물Sodium SulfiteHCID 24437—
반응물Sodium BicarbonateHCID 516892—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물3-Isothiocyanato-4-methoxybenzoic acidHCID 4420630694%

반응 단계

Carbon disulfide (0.26 mL, 4.4 mmol) was added to a mixture comprising 3-amino-4-methoxybenzoic acid (0.25 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 6 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 2.5 hours. Thereafter, 1M hydrochloric acid (1.5 mL) and sodium sulfite (38 mg, 0.30 mmol) were added and mixed. Then, ethyl acetate (6 mL) was added, and the organic layer was separated and concentrated under reduced pressure to dryness. To the obtained residue, ethyl acetate (6 mL), water (2 mL), sodium hydrogencarbonate (6 mg, 0.07 mmol) and sodium sulfite (9 mg, 0.07 mmol) were added, the organic layer was separated and concentrated under reduced pressure to dryness to obtain 3-isothiocyanato-4-methoxybenzoic acid as a colorless solid (0.29 g, yield: 94%, HPLC purity: 99%, HPLC retention time: 3.5 min). LC-MS ES-208 (retention time: 21.6 min, condition 3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367857B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-16fb188c3b9b4fe390f9e99aa88604e7
출처 메모uspto-grants-2013_02