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HRID 1696322作成日:2026年10月27日

Sodium Sulfite → 3-(1-(Tert-butyldimethylsilyloxy)cyclobutyl)propane-1,2-diol

https://huagongshe.com/reaction/1696322

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium SulfiteHCID 24437—
反応物Methyl morpholine oxideHCID 82029—
反応物(1-Allylcyclobutoxy)(tert-butyl)dimethylsilaneHCID 66844818—
反応物2-Methylpropan-2-ol--water (1/1)HCID 71401949—
触媒Osmium TetroxideHCID 30318—
溶媒WaterHCID 962—
生成物3-(1-(Tert-butyldimethylsilyloxy)cyclobutyl)propane-1,2-diolHCID 66845148—

反応手順

To a 2 L round bottomed flask was added (1-allylcyclobutoxy) (tert-butyl)dimethylsilane (previous step) and H2O/t-BuOH (1:1, 1 L). NMO (32.68 g, 279 mmol) was added to the mixture. After stirring for 5 min the solution was found to be homogenous. Osmium tetroxide (1.00 g, 3.93 mmol) was added and the reaction was stirred at RT. After 2 h, TLC revealed the reaction to be complete. 500 mL of H2O and sodium sulfite (19.5 g, 155 mmol) were added and the reaction was stirred for another hour. The aqueous solution was extracted with ether (2×1 L). The combined organics were concentrated in vacuo to give 3-(1-(tert-butyldimethylsilyloxy)cyclobutyl)propane-1,2-diol, as a light yellow oil. The oil contained some t-BuOH, but was carried forward without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08163766B2
出典データセットuspto-grants-2012_04
ORD IDord-7dbd3081f1424549a5625553e636acc7
出典メモuspto-grants-2012_04