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ChemicalBook CAS DataBase List o-Chlorobenzenesulfonamide

o-Chlorobenzenesulfonamide synthesis

8synthesis methods
-

Yield: 99.1%

Reaction Conditions:

with ammonium hydroxide in tetrahydrofuran at 0 - 20; for 2.16667 h;

Steps:

5.1 Step 1
To a solution of 2-chlorobenzene-l-sulfonyl chloride (2.0 g, 9.5 mmol, 1.3 mL) in THF (20.0 mL) was added NH3.H20 (3.3 g, 28.4 mmol, 3.7 mL, 25% solution) at 0°C. The mixture was stirred at 0°C for 10 min and then warmed to 20°C for 2 h. The reaction mixture was concentrated to afford 2-chlorobenzenesulfonamide (1.8 g, 9.4 mmol, 99.1% yield). 1H NMR (400MHz, DMSO-d6) δ 7.96 (dd, J= 1.4, 7.8 Hz, 1H), 7.65 - 7.55 (m, 2H), 7.54 - 7.34 (m, 7H).

References:

QUENTIS THERAPEUTICS, INC.;VACCA, Joseph P.;LI, Dansu;BETTIGOLE, Sarah WO2018/222918, 2018, A1 Location in patent:Paragraph 0199

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