4-Toluenesulfonyl chloride → 6-Phenylhexyl tosylate

참여 물질

역할	이름	HCID	투입량
반응물	4-Toluenesulfonyl chloride	HCID 7397	—
반응물	Triethylamine	HCID 8471	—
반응물	6-Phenyl-1-hexanol	HCID 520110	—
촉매	4-(Dimethylamino)pyridine	HCID 14284	—
생성물	6-Phenylhexyl tosylate	HCID 10688038	81%

반응 단계

This compound was synthesized as a colorless oil from 6-phenylhexan-1-ol (137.0 mg, 0.77 mmol), TsCl (190.7 mg, 1.00 mmol), Et3N (155.0 mg, 1.54 mmol), and DMAP (93.8 mg, 0.77 mmol) in 81% yield by following general procedure 1.1: 1H NMR (400 MHz, CDCl3, δH) 7.87-7.77 (m, 2H), 7.35 (d, J=8.0 Hz, 2H), 7.33-7.24 (m, 2H), 7.23-7.13 (m, 3H), 4.03 (t, J=6.5 Hz, 2H), 2.65-2.53 (m, 2H), 2.45 (s, 3H), 1.75-1.50 (m, 4H), 1.45-1.19 (m, 4H); 13C NMR (100 MHz, CDCl3, 144.93, 142.73, 133.40, 130.08, 128.60, 128.52, 128.11, 125.92, 70.89, 35.99, 31.44, 28.98, 28.78, 25.47, 21.88. ESI-MS: 333.1 (M+H+), 355.1 (M+Na+).

출처 및 근거

DOI	10.6084/m9.figshare.5104873.v1
특허 번호	US09346791B2
출처 데이터셋	uspto-grants-2016_05
ORD ID	ord-ffb79d9b04094fb4b521171772a53091
출처 메모	uspto-grants-2016_05