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HRID 17898作成日:2026年10月23日

Water → 1-(1,3-Dioxaindan-5-yl)cyclopropane-1-carboxylic acid

https://huagongshe.com/ja/reaction/17898

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物1-Bromo-2-ChloroethaneHCID 7849—
反応物Sodium HydroxideHCID 14798—
反応物3,4-(Methylenedioxy)phenylacetonitrileHCID 78178—
触媒Benzyl triethylammonium chlorideHCID 66133—
生成物1-(1,3-Dioxaindan-5-yl)cyclopropane-1-carboxylic acidHCID 1434960880%

反応条件

温度70 °C

反応手順

A mixture of benzo[1,3]dioxole-5-acetonitrile (5.10 g, 31.7 mmol), 1-bromo-2-chloro-ethane (9.00 mL, 109 mmol), and benzyltriethylammonium chloride (0.181 g, 0.795 mmol) was heated at 70° C. and then 50% (wt./wt.) aqueous sodium hydroxide (26 mL) was slowly added to the mixture. The reaction was stirred at 70° C. for 18 hours and then heated at 130° C. for 24 hours. The dark brown reaction mixture was diluted with water (400 mL) and extracted once with an equal volume of ethyl acetate and once with an equal volume of dichloromethane. The basic aqueous solution was acidified with concentrated hydrochloric acid to pH less than one and the precipitate filtered and washed with 1 M hydrochloric acid. The solid material was dissolved in dichloromethane (400 mL) and extracted twice with equal volumes of 1 M hydrochloric acid and once with a saturated aqueous solution of sodium chloride. The organic solution was dried over sodium sulfate and evaporated to dryness to give a white to slightly off-white solid (5.23 g, 80%) ESI-MS m/z calc. 206.1. found 207.1 (M+1)+. Retention time of 2.37 minutes. 1H NMR (400 MHz, DMSO-d6) δ 1.07-1.11 (m, 2H), 1.38-1.42 (m, 2H), 5.98 (s, 2H), 6.79 (m, 2H), 6.88 (m, 1H), 12.26 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741321B2
出典データセットuspto-grants-2010_06
ORD IDord-16c41d8ea400486091d9c5dbdaba818c
出典メモuspto-grants-2010_06