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HRID 1243962作成日:2026年10月26日

Methyl iodide → Diphenoxymethane

https://huagongshe.com/reaction/1243962

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物TetrahydrofuranHCID 8028—
反応物4-PhenoxyphenolHCID 13254—
反応物Potassium tert-butoxideHCID 23665647—
生成物DiphenoxymethaneHCID 78183—

反応手順

4-(Phenoxy)phenol (9.31 g, 50 mmol) in THF (100 mL) was treated with potassium t-butoxide (6.17 g, 55 mmol) at room temperature for 10 min. Methyl iodide (7.87 g, 55 mmol) was added by syringe. After stirring for 18 h at room temperature the reaction was quenched with saturated ammonium chloride solution and diluted with ethyl ether. The separated organic layer was washed with saturated ammonium chloride solution, dried with magnesium sulfate, filtered and concentrated to give 9.98 g of the title compound as a pale yellow oil. GS-MS (m/z, EI): 200 [M]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07119201B2
出典データセットuspto-grants-2006_10
ORD IDord-191aa6473abc48819fccfa42a9fa38cc
出典メモuspto-grants-2006_10