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HRID 385175作成日:2026年10月25日

Hydrochloric Acid → 4-Isothiocyanatobenzoic acid

https://huagongshe.com/reaction/385175

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物IodineHCID 807—
反応物4-Aminobenzoic AcidHCID 978—
反応物Carbon DisulfideHCID 6348—
反応物TriethylamineHCID 8471—
反応物Sodium SulfiteHCID 24437—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物4-Isothiocyanatobenzoic acidHCID 242946100%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367857B2
出典データセットuspto-grants-2013_02
ORD IDord-ab2b50207f4f43b9b58b852686443ab6
出典メモuspto-grants-2013_02