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HRID 63809作成日:2026年10月24日

Acetic Acid → 7,9,10-Trimethyl-2,4-dipropyl-7-(4,8,12-trimethyl-tridecyl)-4,5,6,7-tetrahydro-1,3,8-trioxa-phenanthrene

https://huagongshe.com/ja/reaction/63809

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物ButanalHCID 261—
反応物Ethyl AcetateHCID 8857—
反応物(+)-gamma-TocopherolHCID 92729—
触媒Sulfuric AcidHCID 1118—
溶媒WaterHCID 962—
生成物7,9,10-Trimethyl-2,4-dipropyl-7-(4,8,12-trimethyl-tridecyl)-4,5,6,7-tetrahydro-1,3,8-trioxa-phenanthreneHCID 68497100100%

反応手順

A 25 mL RBF was charged with butyraldehyde (155 mg, 2.16 mmol), AcOH (2 mL) and H2SO4 (1 drop). To the flask was then added a solution of (+)-γ-tocopherol (Ex-1C-1) (300 mg, 0.72 mmol) in AcOH (3 mL) dropwise over 2 h via syringe pump. The reaction was then stirred for 16 h and monitored by TLC (9:1 Hept:EtOAc). The reaction was then diluted with water (15 mL) and extracted with DCM (3×20 mL). The combined organic layers were washed with water (3×15 mL), dried over Na2SO4, filtered and concentrated by rotary evaporation to yield 7,9,10-trimethyl-2,4-dipropyl-7-(4,8,12-trimethyl-tridecyl)-4,5,6,7-tetrahydro-1,3,8-trioxa-phenanthrene (Ex-1C-2) as a brownish oil (425 mg, >100%), which was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447006B2
出典データセットuspto-grants-2016_09
ORD IDord-128bc00887994050a25505632883fba9
出典メモuspto-grants-2016_09