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HRID 52804作成日:2026年10月24日

Allyl Alcohol → Allyl 2,2,2-Trichloroacetimidate

https://huagongshe.com/ja/reaction/52804

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl AlcoholHCID 7858—
反応物TrichloroacetonitrileHCID 11011—
反応物Sodium hydrideHCID 24758—
溶媒Diethyl EtherHCID 3283—
生成物Allyl 2,2,2-TrichloroacetimidateHCID 316905—

反応手順

A suspension of 80% sodium hydride (945 mg., 31.5 mmol.; washed twice with 25 ml. of hexane) in dry. ether (30 ml.) was treated dropwise with a solution of 2-propen-1-ol (21.4 ml., 18.3 g., 315 mmol.), in dry ether (45 ml.), stirred for 20 minutes at room temperature under argon and then cooled to 0° C. (ice-salt bath). Trichloroacetonitrile (30 ml. or 42.3 g., 0.30 mole) was added over a period of 15 minutes and the brownish solution was stirred at 0° C. for 40 minutes, at 10° C. for 10 minutes and at room temperature for 10 minutes. The reaction mixture was concentrated to a syrup, treated with a solution of methanol (1.2 ml.) in pentane (30 ml.) and stirred vigorously for 5.0 minutes. The light brown precipitates were filtered off, washed with pentane (2×30 ml.) and the combined flitrates concentrated down to a light brown liquid. The liquid was redissolved in pentane (30 ml.), stirred for a few minutes, and the resulting suspension filtered, and the precipitates obtained washed with pentane (30 ml.), repeating the procedure at least one more time. The clear filtrate was concentrated and dried in vacuo to give 54.0 g. of title compound as a light red-colored liquid. This material was stored as a solution in hexane at 10° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05616775
出典データセットuspto-grants-1997_04
ORD IDord-9e9a32d3f05b4785a023b7a85defd590
出典メモuspto-grants-1997_04