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HRID 252218作成日:2026年10月27日

Ammonia → Tert-butyl 3-sulfamoylbenzoate

https://huagongshe.com/reaction/252218

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Sulfuric AcidHCID 1118—
反応物tert-ButanolHCID 6386—
反応物Sulfuric acid magnesium salt (1:1)HCID 24083—
反応物Benzoic acid, 3-(chlorosulfonyl)-HCID 77641—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物Tert-butyl 3-sulfamoylbenzoateHCID 5973369542.9%

反応条件

温度0 °C

反応手順

Sulfuric acid (conc., 498 μL, 9.06 mmol) was added to a suspension of MgSO4 (4.36 g, 36.22 mmol) in CH2Cl2 (36 mL). The reaction mixture was stirred for 15 minutes, treated with 3-chlorosulfonyl-benzoic acid (Aldrich, 2 g, 9.06 mmol) and 2-methyl-propan-2-ol (anhydrous, 4.33 mL, 45.27 mmol), capped tightly, and stirred overnight at room temperature. The next day, the mixture was cooled to 0° C., treated with 7N NH3 in methanol (Aldrich, 40 mL) dropwise, and stirred for 30 minutes. The solvents were removed in vacuo and the crude was dissolved in ethyl acetate and saturated NaHCO3. The organic layer was washed with saturated NaHCO3, water, and brine, dried over MgSO4, filtered, and concentrated in vacuo to afford the title compound as a white solid (1 g, 42.9% yield). 1H-NMR (CDCl3): δ 8.51-8.53 (m, 1H), 8.20-8.21 (m, 1H), 8.08-8.11 (m, 1H), 7.57-7.62 (m, 1H), 5.09 (bs, 2H), and 1.61 (s, 9H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07868023B2
出典データセットuspto-grants-2011_01
ORD IDord-5cf8e981a9a04de19c96d38c95f3a4b8
出典メモuspto-grants-2011_01