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HRID 2112438作成日:2026年10月27日

3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid → 3-(4-Hydroxy-3-methoxyphenyl)-2-propenoic acid 4-bromobutyl ester

https://huagongshe.com/reaction/2112438

反応式

関与物質

役割名称HCID仕込み量
反応物3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic AcidHCID 709—
反応物TetrahydrofuranHCID 8028—
反応物Carbon tetrabromideHCID 11205—
生成物3-(4-Hydroxy-3-methoxyphenyl)-2-propenoic acid 4-bromobutyl esterHCID 53938916265.4%

反応手順

To a solution of 3- (4-hydroxy-3-methoxyphenyl) -2-propenoic acid (10 g, 51.5 mmoles) in THF (400 ml) triphenylphosphine (2.7 g, 10.3 mmoles) and carbon tetrabromide (34.16 g, 10.3 mmoles) are added and the solution is left at room temperature, under magnetic stirring, for 48 hours. The solid is filtered and then evaporated at reduced pressure. The obtained crude product is purified by chromatogrphy on silica gel eluting with n-hexane/ethyl acetate 7/3. 9 g of 3-(4-hydroxy-3-methoxyphenyl)-2-propenoic acid 4-bromobutyl ester are obtained. M.p.=86-89° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07524836B2
出典データセットuspto-grants-2009_04
ORD IDord-0bf0c2072d8f452d81e003b7d4279ad3
出典メモuspto-grants-2009_04