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HRID 232750作成日:2026年10月26日

Trimethyl borate → Boronic acid, (4-ethylphenyl)-

https://huagongshe.com/reaction/232750

反応式

関与物質

役割名称HCID仕込み量
反応物Trimethyl borateHCID 8470—
反応物1-Bromo-4-ethylbenzeneHCID 15313—
反応物MagnesiumHCID 5462224—
溶媒Diethyl EtherHCID 3283—
生成物Boronic acid, (4-ethylphenyl)-HCID 273435241%

反応手順

A solution of 1-bromo-4-ethyl benzene (2.0 g, 11 mmol) in dry ether (5 ml) was added to magnesium turnings (311 mg, 13 mmol), which had been suspended in dry ether, by a dropwise addition. After addition was complete, the suspension was refluxed for a period of 15 min after which nearly all of the magnesium had reacted. This solution was then added to trimethy borate (1.12 g, 11 mmol) previously dissolved in ether (5 ml) at -78° C., the solution was warmed to room temperature and stirred for 90 min. The reaction was quenched by the addition of 10% aqueous HCl (2 ml) and the solution was extracted with ether. The combined ether extracts was extracted with 1M NaOH (2×20 ml), the aqueous extracts were acidified with dilute HCl to pH 2 and extracted with ether (2×25 ml). The combined ether extracts was washed once with water (10 ml), dried and evaporated to produce a white solid (676 mg, 38% yield), m.p. 138°-140° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05591761
出典データセットuspto-grants-1997_01
ORD IDord-c1c147a2cbeb4858ba5715228f5b065a
出典メモuspto-grants-1997_01