戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1811021作成日:2026年10月25日

Trifluoromethanesulfonic anhydride → 8-Methyl-2-phenylchroman-7-yl trifluoromethanesulfonate

https://huagongshe.com/reaction/1811021

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoromethanesulfonic anhydrideHCID 67749—
反応物8-Methyl-2-phenylchroman-7-olHCID 14224896—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物8-Methyl-2-phenylchroman-7-yl trifluoromethanesulfonateHCID 5937501689%

反応手順

Step 2 Trifluoromethanesulfonic anhydride (0.613 mL, 3.63 mmol) was added dropwise to a solution of 8-methyl-2-phenylchroman-7-ol (671 mg, 2.79 mmol) in DCM (10 mL) and pyridine (10 mL) at 0° C. After 30 min, the mixture was diluted with EtOAc (70 mL), washed with water (2×30 mL) and brine (30 mL), dried and concentrated. The residue was purified by column chromatography (eluting with a gradient from 95:5 to 85:15 hexane-EtOAc) to give 8-methyl-2-phenylchroman-7-yl trifluoromethanesulfonate as colorless liquid (925 mg, 89%). 1H NMR (400 MHz, chloroform-d) δ 7.28-7.61 (5 H, m), 6.97 (1 H, d, J=8.58 Hz), 6.79 (1 H, d, J=8.58 Hz), 5.11 (1 H, dd, J=10.23, 2.31 Hz), 2.99 (1 H, ddd, J=16.73, 11.11, 5.83 Hz), 2.68-2.88 (1 H, m), 2.17-2.32 (4 H, m), 1.88-2.12 (1 H, m). Mass spectrum m/z 390.0 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08362065B2
出典データセットuspto-grants-2013_01
ORD IDord-19f48af94e0f445ca3f01124d53e5904
出典メモuspto-grants-2013_01