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HRID 245890作成日:2026年10月26日

Tert-Butanesulfinamide → (NE)-2-methyl-N-(1,3-oxazol-2-ylmethylidene)propane-2-sulfinamide

https://huagongshe.com/reaction/245890

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-ButanesulfinamideHCID 3382465—
反応物1,3-Oxazole-2-carboxaldehydeHCID 14786609—
触媒Titanium tetraethoxideHCID 76524—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物(NE)-2-methyl-N-(1,3-oxazol-2-ylmethylidene)propane-2-sulfinamideHCID 8942102068%

反応手順

In a round-bottomed flask, oxazole-2-carbaldehyde (300 mg, 3.09 mmol) was dissolved in THF (7 ml) and 2-methylpropane-2-sulfinamide (450 mg, 3.71 mmol) and titanium(IV) ethoxide (1.3 ml, 6.18 mmol) were added. The reaction mixture was stirred at room temperature overnight then slowly quenched by dropwise addition of brine (2 ml) which resulted in the formation of a thick yellow precipitate. The reaction mixture was diluted with ethyl acetate and stirred vigorously at room temperature for 10 min. The suspension was filtered over Celite and rinsed with ethyl acetate. The filtrate was concentrated and the residue was chromatographed over silica gel with EtOAc/hexanes (gradient 0-30% EtOAc) to afford 419 mg (68%) of 2-methyl-propane-2-sulfinic acid 1-oxazol-2-yl-meth-(E)-ylideneamide as a light yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08658646B2
出典データセットuspto-grants-2014_02
ORD IDord-8287c727cc9445aca7984ddd80b97e49
出典メモuspto-grants-2014_02