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HRID 750550作成日:2026年10月26日

Ethyl Bromide → Methyl 9-ethylxanthene-9-carboxylate

https://huagongshe.com/reaction/750550

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl BromideHCID 6332—
反応物methyl 9H-xanthene-9-carboxylateHCID 699662—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 9-ethylxanthene-9-carboxylateHCID 68962313—

反応手順

10.0 g (0.042 mol) of methyl 9-xanthenecarboxylate (obtainable according to step 1.1.a) are dissolved in 100 mL of tetrahydrofuran and combined batchwise with 5.16 g (0.044 mol) of potassium tert-butoxide while cooling. Then at about 18° C. to 22° C., 6.296 mL (0.083 mol) of bromoethane are added dropwise; after it has all been added, the mixture is stirred for about 1.5 hours at ambient temperature. The precipitate formed is suction filtered and the solvent is removed by distillation. The residue remaining is taken up in diethyl ether and extracted with water. The organic phase is dried over magnesium sulfate and the solvent is removed by distillation. The crude product obtained is used in the next step without any further purification. Yield: 7.92 g of yellow oil (70% of theoretical yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07405224B2
出典データセットuspto-grants-2008_07
ORD IDord-d4816aa31f8c4b9b84fc990dd7d05bb4
出典メモuspto-grants-2008_07