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HRID 548663作成日:2026年10月24日

Imidazole → (2R)-1-{[Tri(propan-2-yl)silyl]oxy}propan-2-ol

https://huagongshe.com/ja/reaction/548663

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物Triisopropylsilyl chlorideHCID 139400—
反応物R-(-)-1,2-PropanediolHCID 259994—
溶媒DimethylformamideHCID 6228—
生成物(2R)-1-{[Tri(propan-2-yl)silyl]oxy}propan-2-olHCID 5750469776.7%

反応手順

Triisopropylsilyl chloride (83.8 mL, 390 mmol) was added slowly over 15 minutes to a solution of (2R)-propane-1,2-diol (29.7 g, 390 mmol) in DMF at 0° C. (100 mL) keeping the internal temperature below 15° C. This was followed by addition of imidazole (66.4 g, 975 mmol) and the reaction mixture was allowed to warm to RT and stirred under argon for 20 hours. The reaction was quenched with 1M hydrochloric acid/diethyl ether (300 mL/800 mL). The organic layer was separated and washed with 1M hydrochloric acid followed by saturated brine solution. The organic layer was dried (MgSO4), filtered and evaporated. Purification by distillation at 10 mmHg, 90-104° C., afforded the title compound as colourless oil (69.5 g). 1H NMR δ (CDCl3): 1.05 (s, 18H), 1.05-1.1 (m, 3H), 1.05 (d, 3H), 2.55 (s, 1H), 3.45 (dd, 1H), 3.7 (dd, 1H), 3.85 (m, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07943607B2
出典データセットuspto-grants-2011_05
ORD IDord-de60c933bb20461e8d928c429980b33b
出典メモuspto-grants-2011_05