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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 992590생성일: 2026년 10월 27일

Hydrochloric Acid → 2-{2-[N-(2-methyl-2-sulfanylpropyl)carbamoyl]phenyl}benzoic acid

https://huagongshe.com/reaction/992590

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TriethylamineHCID 8471—
반응물Diphenic anhydrideHCID 72794—
반응물1-Amino-2-methyl-2-propanethiol hydrochlorideHCID 13049104—
용매DichloromethaneHCID 6344—
생성물2-{2-[N-(2-methyl-2-sulfanylpropyl)carbamoyl]phenyl}benzoic acidHCID 1841279899.8%

반응 단계

To an ice-cooled suspension of 1-amino-2-methyl-2-propanethiol hydrochloride (1.08 g, 7.62 mmol) in methylene chloride (20 mL) was added triethylamine (1.2 mL, 8.61 mmol) followed by dibenzo[c,e]oxepin-5,7-dione (1.68 g, 7.42 mmol). After stirring at room temperature for 1 h, cold 2 N HCl (50 mL) was added. After separation, the aqueous layer was extracted with dichloromethane (2×15 mL). The combined organic layers were washed with brine and dried under sodium sulfate. The solvent was removed and the resulting residue was triturated with hexane to give the title compound as white solid (2.44 g, 98.9%). mp 150-153° C.; 1H NMR (CDCl3, 300 MHz): δ1.03 (s, 3H), 1.12 (s, 3H), 1.36 (s, 1H), 3.15 (dd, J=13.7 and 5.7 Hz, 1H), 3.38 (dd, J=13.7 and 6.9 Hz, 1H), 6.92 (t, J=6.1 Hz, 1H), 7.09-7.17 (m 2H), 7.38-7.48 (m, 4H), 7.57-7.61 (m, 1H), 7.80-7.83 (m, 1H); 13C NMR (CDCl3, 75 MHz,): δ29.36, 29.75, 44.66, 53.01, 127.28, 127.96, 128.04, 129.38, 129.93, 130.06, 130.20, 131.19, 132.02, 134.69, 138.90, 140.11, 170.99, 171.24; LCMS (m/e): 330 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06469065B1
출처 데이터셋uspto-grants-2002_10
ORD IDord-31a34c28163c468a9ba5ea74de995ad3
출처 메모uspto-grants-2002_10