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HRID 1712251作成日:2026年10月25日

Hydrochloric Acid → (4-Allyloxy-3-nitrophenyl)methanol

https://huagongshe.com/reaction/1712251

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium borohydrideHCID 4311764—
反応物4-Allyloxy-3-nitrobenzaldehydeHCID 22401152—
溶媒MethanolHCID 887—
生成物(4-Allyloxy-3-nitrophenyl)methanolHCID 29006117—

反応手順

The solution of 2.4 g of 4-allyloxy-3-nitrobenzaldehyde in 30 ml of methanol is cooled to 0° C. with stirring and subsequently admixed with 0.48 g of sodium borohydride in portions over 5 minutes. The reaction mixture is stirred further at 0° C. over 30 minutes, then poured onto cooled 2N HCl (100 ml) and extracted with tert-butyl methyl ether (2×100 ml). The organic phases are washed with water (100 ml), 1M sodium hydrogencarbonate solution (100 ml) and brine (100 ml), dried over sodium sulphate, filtered and concentrated by evaporation. The title compound is obtained as a slightly yellowish oil from the residue by means of flash chromatography (SiO2 60F). Rf=0.12 (1:1 EtOAc-heptane); Rt=3.37.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07790715B2
出典データセットuspto-grants-2010_09
ORD IDord-6ce231f443804a51b30a32f22725ea3a
出典メモuspto-grants-2010_09