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HRID 50102作成日:2026年10月25日

Toluene → HCID 178500902、化合物

https://huagongshe.com/reaction/50102

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物4-FluorobenzonitrileHCID 14517—
反応物Tin tetrachlorideHCID 24287—
反応物Methyl 4-methyl-3-oxopentanoateHCID 2759969—
溶媒HexaneHCID 8058—
生成物HCID 178500902HCID 17850090275.2%

反応条件

温度80 °C

反応手順

75.09 g of methyl isobutyrylacetate (0.50 mol, concentration 96%) and 61.80 g of 4-fluorobenzonitrile (0.50 mol, concentration 98%) were introduced into [500 ml of toluene and treated with 144.7 g of tin tetrachloride (0.55 mol, concentration 99%) at room temperature over the course of 16 min. After half an hour at room temperature, the thick suspension was heated to 80° C. After. 3 h, 175 ml of toluene were distilled off at normal pressure, and the mixture was cooled to room temperature and treated with 450 ml of saturated sodium carbonate and 300 ml of ethyl acetate. The organic phase was separated off and the aqueous phase (after dilution with 300 ml of water) was again extracted with 300 ml of ethyl acetate. After drying the combined organic phases over sodium sulphate, the solvent was removed in vacuo (40° C./25 mbar). 127.2 g of crude product were obtained in the form of a slightly yellowish solid, which was dissolved in 160 ml of n-hexane (slightly turbid solution). After hot filtration and subsequent cooling in an ice bath, 99.8 g of methyl 2-[1-amino-1-(4-fluorophenyl)-methylene]-4-methyl-3-oxopentanoate were obtained after filtration in the form of a pale yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710178B2
出典データセットuspto-grants-2004_03
ORD IDord-1f1b485b281146ec8dd6dd9e597da9cf
出典メモuspto-grants-2004_03