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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 521740생성일: 2026년 10월 25일

Triethylamine → (R)-N-(2-phenylpropyl)propane-2-sulfonamide

https://huagongshe.com/reaction/521740

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-Propanesulfonyl chlorideHCID 82408—
반응물2-Phenylpropylamine hydrochlorideHCID 89332—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물(R)-N-(2-phenylpropyl)propane-2-sulfonamideHCID 2189341586%

반응 단계

To a solution of 2-phenyl-propylamine HCl salt (1.0 g, 5.8 mmol), DMAP (35 mg, 0.3 mmol) and Et3N (1.77 g, 17.5 mmol) in DCM (25 mL) was added propane-2-sulfonyl chloride (1.25 g, 8.7 mmol) dropwise at 0° C. The mixture was stirred at r.t. for 16 h, and was then concentrated under vacuum. The residue was partitioned between EtOAc (100 mL) and H2O (10 mL). The organic layer was separated and washed with brine (10 mL), dried over anhydrous Na2SO4, filtrated and concentrated to give an oil residue. This residue was purified with silica gel column (Hexane/EtOAc=2/1 to 1/1) to obtain the desired product (1.2 g, 86%) as a pale yellow oil. 1H NMR (600 MHz, CDCl3) δ 7.30-7.32 (m, 2H), 7.18-7.24 (m, 3H), 3.90-3.94 (m, 1H), 3.30-3.35 (m, 1H), 3.18-3.22 (m, 1H), 2.99-3.04 (m, 1H), 2.91-2.95 (m, 1H), 1.27 (d, 3H, J=7.2 Hz), 1.25 (d, H, J=7.8 Hz), 1.22 (d, 1H, J=7.2 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09328125B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-3b0e97b9696448e195819d4c87ec5f59
출처 메모uspto-grants-2016_05