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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1158461생성일: 2026년 10월 26일

2-Methyl-2-butene → 2-Chloro-4-methoxy-5-(3-methoxy-propoxy)-benzoic acid

https://huagongshe.com/reaction/1158461

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-2-buteneHCID 10553—
반응물t-Butanol dichloromethaneHCID 18914702—
반응물Sodium ChloriteHCID 23668197—
반응물2-Chloro-4-methoxy-5-(3-methoxy-propoxy)-benzaldehydeHCID 59224010—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
용매Acetonitrile--water (1/1)HCID 18373917—
생성물2-Chloro-4-methoxy-5-(3-methoxy-propoxy)-benzoic acidHCID 59512237—

반응 단계

To a solution of 2-chloro-4-methoxy-5-(3-methoxy-propoxy)-benzaldehyde (1.08 g, 3.55 mmol) in a 3:1 mixture of tert-butanol/CH2Cl2 (20 mL) is added 2-methyl-2-butene (0.74 g, 5.32 mmol), followed by dropwise addition of a solution of NaClO2 (0.67g, 7.10 mmol) and NaH2PO4 (0.67 g, 4.26 mmol) in water (14 mL) over 15 min at room temperature, and stirring is continued overnight. The reaction mixture is poured into ice/saturated aqueous NaHCO3 solution, the water phase is washed with AcOEt. The ice-cold aqueous layer is acidified with HCl 37% to form a white precipitate which is filtered off, washed with ice-cold water and dried in vacuo. The compound is obtained as white solid. MS: 273.0 [M−H]+. tR (HPLC, Nucleosil C18HD column, 20-100% CH3CN/H2O/6 min, 100% CH3CN/2 min, CH3CN and H2O containing 0.1% TFA, flow: 1 mL/min): 3.25 min. 1H-NMR (CDCl3): δ 1.96 (m, 2H), 3.25 (s, 3H), 3.47 (m, 2H), 3.85 (s, 3H), 4.03 (m, 2H), 7.10 (s, 1H), 7.39 (s, 1H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07807709B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-c8ed2c8768744fa8aef40a50a880b3f2
출처 메모uspto-grants-2010_10