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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 385185생성일: 2026년 10월 24일

Hydrochloric Acid → 3,5-Diisothiocyanatobenzoic acid

https://huagongshe.com/ko/reaction/385185

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물IodineHCID 807—
반응물Carbon DisulfideHCID 6348—
반응물TriethylamineHCID 8471—
반응물3,5-Diaminobenzoic acidHCID 12062—
반응물Sodium SulfiteHCID 24437—
반응물Sodium BicarbonateHCID 516892—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물3,5-Diisothiocyanatobenzoic acidHCID 61684186%

반응 단계

Carbon disulfide (0.54 mL, 9.1 mmol) was added to a mixture comprising 3,5-diaminobenzoic acid (0.23 g, 1.5 mmol), tetrahydrofuran (1.0 mL), water (1.0 mL) and triethylamine (0.84 mL, 6.0 mmol), followed by stirring at room temperature for 31 hours. To the obtained reaction mixture, a tetrahydrofuran (2.0 mL) solution of iodine (0.82 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 (76 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 (3 mL) and sodium hydrogencarbonate (10 mg, 0.12 mmol) were added, and the organic layer was concentrated under reduced pressure to dryness. To the obtained residue, chloroform (6 mL) was added and thoroughly mixed, and then an insoluble matter was removed by filtration. The filtrate was concentrated under reduced pressure to dryness, and then, to the obtained residue, chloroform (6 mL) and hexane (1 mL) were added and thoroughly mixed. Then, the insoluble matter was removed by filtration. The filtrate was concentrated under reduced pressure to dryness to obtain 3,5-diisothiocyanatobenzoic acid as a colorless solid (0.31 g, yield: 86%, HPLC purity: 97%, HPLC retention time: 5.3 min). LC-MS ES-235 (retention time: 4.6 min, condition 1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367857B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-f54a88d5240f4554a96059712d0a7fe3
출처 메모uspto-grants-2013_02