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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39441생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/39441

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1-Bromo-2-ChloroethaneHCID 7849—
반응물Sodium HydroxideHCID 14798—
반응물3,4-(Methylenedioxy)phenylacetonitrileHCID 78178—
촉매Benzyl triethylammonium chlorideHCID 66133—
생성물1-(1,3-Dioxaindan-5-yl)cyclopropane-1-carboxylic acidHCID 1434960880%

반응 조건

온도70 °C

반응 단계

A mixture of 2-(benzo[d][1,3]dioxol-5-yl)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 24 hours and then heated at 130° C. for 48 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 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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524910B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-a386349425554e0389c89cfea7482ea7
출처 메모uspto-grants-2013_09