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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 385175생성일: 2026년 10월 23일

Hydrochloric Acid → 4-Isothiocyanatobenzoic acid

https://huagongshe.com/ko/reaction/385175

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물IodineHCID 807—
반응물4-Aminobenzoic AcidHCID 978—
반응물Carbon DisulfideHCID 6348—
반응물TriethylamineHCID 8471—
반응물Sodium SulfiteHCID 24437—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물4-Isothiocyanatobenzoic acidHCID 242946100%

반응 단계

Carbon disulfide (0.66 mL, 11 mmol) was added to a mixture comprising 4-aminobenzoic acid (0.50 g, 3.6 mmol), tetrahydrofuran (2.5 mL), water (2.5 mL) and triethylamine (1.3 mL, 9.1 mmol), followed by stirring at room temperature for 24 hours. To the obtained reaction mixture, a tetrahydrofuran (2.5 mL) solution of iodine (1.0 g, 4.0 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 (3.6 mL) and sodium sulfite (91 mg, 0.72 mmol) were added and stirred. Then, ethyl acetate (15 mL) was added, and the organic layer was separated and concentrated under reduced pressure to dryness. To the residue, ethyl acetate (5 mL) and hexane (5 mL) were added and thoroughly mixed, and then, the insoluble matter was collected by filtration to obtain 4-isothiocyanatobenzoic acid as a colorless solid (0.65 g, yield: 100%, HPLC purity: 92%, HPLC retention time: 3.7 min). LC-MS ES-178 (retention time: 4.0 min, condition 1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367857B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-ab2b50207f4f43b9b58b852686443ab6
출처 메모uspto-grants-2013_02