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HRID 863595作成日:2026年10月26日

Triphenylphosphine → 3-[4-(2-Methyltetrazol-5-yl)-2,6-dimethylphenoxy]-propylbromide

https://huagongshe.com/reaction/863595

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物3-Bromo-1-propanolHCID 12308—
反応物Win 58768HCID 148372—
反応物Diethyl azodicarboxylateHCID 5462977—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物3-[4-(2-Methyltetrazol-5-yl)-2,6-dimethylphenoxy]-propylbromideHCID 1539152382%

反応条件

温度0 °C

反応手順

A mixture of (3-hydroxypropyl)-bromide (2.17 ml, 24 mmol), 4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenol (5.1 g, 25 mmol), and DEAD (4.18 g, 24 mmol) was dissolved in 50 ml of THF at 0° C. To the above solution was added dropwise triphenylphosphine (6.3 g, 24 mmol) at 0° C. and the mixture was allowed to stir at 0° C. for 0.5 h. The mixture was diluted with 500 ml of water and 100 ml of ether, and the aqueous layere was extracted with ether (2×400 ml). The combined organic layer was dried over sodium sulfate, and concentrated in vacuo. The residue was dissolved in 800 ml of ether, and the organic layer was washed with 10% NaOH solution (3×50 ml), dried over sodium sulfate, and concentrated in vacuo. The residue was purified by silica column chromatography (7 cm column, ethyl acetate/hexane, 1/5) followed by recrystallization from methylene chloride/hexane to afford 6.4 g (82%) of 3-[4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenoxy]-propylbromide, as a light yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05721261
出典データセットuspto-grants-1998_02
ORD IDord-792e706ecee04535a5e151d198656c3c
出典メモuspto-grants-1998_02