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HRID 709484作成日:2026年10月24日

Borane;tetrahydrofuran → 2-(4-Hydroxymethyl-phenylsulfanylmethyl)-benzoic acid 2,2,2-trichloro-ethyl ester

https://huagongshe.com/ja/reaction/709484

反応式

関与物質

役割名称HCID仕込み量
反応物Borane;tetrahydrofuranHCID 2723981—
反応物2-(4-Carboxy-phenylsulfanylmethyl)-benzoic acid 2,2,2-trichloro-ethyl esterHCID 66865243—
溶媒TetrahydrofuranHCID 8028—
生成物2-(4-Hydroxymethyl-phenylsulfanylmethyl)-benzoic acid 2,2,2-trichloro-ethyl esterHCID 6686525491%

反応条件

温度0 °C

反応手順

To a solution of 2-(4-Carboxy-phenylsulfanylmethyl)-benzoic acid 2,2,2-trichloro-ethyl ester (80 mg, 0.191 mmol) in THF (1 mL) at 0° C. was added dropwise BH3-THF (0.4 mL, 1.0M solution in THF). The reaction was stirred at 0° C. for 0.5 h after the addition was complete, thereafter the cooling bath was removed and the reaction was stirred for 2 h at rt. The reaction was quenched at 0° C. by careful addition of THF/H2O, 80/20 followed by dropwise addition of 2M HCl. The mixture was stirred for an additional 10 minutes and thereafter diluted with water. THF was removed and the water phase was extracted with DCM and the combined organic phase was dried through a phase separator and concentrated to give the titled compound (70 mg, 91%) as an oil; 1H NMR (400 MHz, CDCl3): δ 4.53 (s, 2H), 4.64 (s, 2H), 4.94 (s, 2H), 7.19-7.30 (m, 5H), 7.30-7.36 (m, 1H), 7.37-7.44 (m, 1H), 8.06 (d, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181181B2
出典データセットuspto-grants-2015_11
ORD IDord-1917137476da45608302e5ee2555c87b
出典メモuspto-grants-2015_11