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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 385177생성일: 2026년 10월 25일

Hydrochloric Acid → Benzoic acid, 3-isothiocyanato-

https://huagongshe.com/reaction/385177

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물IodineHCID 807—
반응물Carbon DisulfideHCID 6348—
반응물3-Aminobenzoic AcidHCID 7419—
반응물TriethylamineHCID 8471—
반응물Sodium SulfiteHCID 24437—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물Benzoic acid, 3-isothiocyanato-HCID 7504696%

반응 단계

Carbon disulfide (0.26 mL, 4.4 mmol) was added to a mixture comprising 3-aminobenzoic acid (0.20 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 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 mixed. Then, ethyl acetate (6 mL) was added, and the organic layer was separated and concentrated under reduced pressure to dryness. To the residue, ethyl acetate (4 mL) and water (2 mL) were added, and the organic layer was concentrated under reduced pressure to dryness to obtain 3-isothiocyanatobenzoic acid as a cream-colored solid (0.25 g, yield: 96%, HPLC purity: 95%, HPLC retention time: 3.6 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-b508ba08c944470eb23b513138902056
출처 메모uspto-grants-2013_02