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HRID 461444作成日:2026年10月26日

Water → 2,3-Bis(1-phenyl-1-hydroxymethyl)naphthalene

https://huagongshe.com/reaction/461444

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2,3-NaphthalenedicarboxaldehydeHCID 96400—
反応物HCID 178418255HCID 178418255—
溶媒TetrahydrofuranHCID 8028—
生成物2,3-Bis(1-phenyl-1-hydroxymethyl)naphthaleneHCID 2139375086.6%

反応手順

2,3-Naphthalenedicarboxaldehyde (10.0 g) in dry tetrahydrofuran (100ml) was added to phenylmagnesium bromide [derived from bromobenzene (53 g) and magnesium (8 g)] in dry tetrahydrofuran (500 ml) over 1 hr. and the solution was refluxed for a further 3 hr. On cooling, water (500 ml) was added and the ethereal layer was decanted. The aqueous slurry was washed with ether (4 × 500 ml) and the combined ethereal extracts were dried (magnesium sulphate) and evaporated to dryness. The residue was purified by chromatography on silica gel and recrystallised from dichloromethane/petroleum ether (b.p. 40°-60°) to yield two isomers of 2,3-bis(1-phenyl-1-hydroxymethyl)naphthalene (III) (8.0 g. m.p. 145° and 3.0 g, m.p. 164°).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04062955
出典データセットuspto-grants-1977_12
ORD IDord-ec42555b67f34b5e82c0293fffbf1762
出典メモuspto-grants-1977_12