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HRID 569628作成日:2026年10月26日

4-Methoxystyrene → (1RS,2SR)-1-cyano-1,2,3,4-tetrahydro-2-p-methoxyphenylnaphthalene

https://huagongshe.com/reaction/569628

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethoxystyreneHCID 12507—
反応物1-Cyano-4-methoxybenzocyclobuteneHCID 18690136—
溶媒1,2-DichlorobenzeneHCID 7239—
生成物(1RS,2SR)-1-cyano-1,2,3,4-tetrahydro-2-p-methoxyphenylnaphthaleneHCID 67945262—

反応手順

A solution of 1-cyano-4-methoxybenzocyclobutene (7.5 g.; described in the Journal of the American Chemical Society, 1976, 98, 8185) and p-methoxystyrene (11.1 g.) in o-dichlorobenzene (40 ml.) was heated under reflux for 30 minutes under an atmosphere of argon and then evaporated to dryness, and the residue was purified by chromatography on a silica gel column using a 20:1 v/v mixture of toluene and ethyl acetate as eluant. A mixture of a solution of the residue (12.0 g.) in toluene (200 ml.), a solution of sodium hydroxide (20 g.) in water (200 ml.) and 40% w/v aqueous tetrabutylammonium hydroxide solution (1 ml.) was stirred vigorously under an atmosphere of argon at laboratory temperature for 12 hours and the layers were then separated. The aqueous layer was extracted twice with diethyl ether (100 ml. each time) and the combined organic solutions were washed with water, dried and evaporated to dryness. There was thus obtained as residue (1RS,2SR)-1-cyano-1,2,3,4-tetrahydro-2-p-methoxyphenylnaphthalene, m.p. 126°-131° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04732912
出典データセットuspto-grants-1988_03
ORD IDord-18cc9d7647234378a45f353951795880
出典メモuspto-grants-1988_03