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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2246759생성일: 2026년 10월 27일

Hydrochloric Acid → 4-Hexyl-2-methoxy-1-phenoxybenzene

https://huagongshe.com/reaction/2246759

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-Chloro-2-methoxy-1-phenoxybenzeneHCID 58604131—
반응물HCID 178444611HCID 178444611—
촉매ZincchlorideHCID 3007855—
촉매HCID 178418851HCID 178418851—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물4-Hexyl-2-methoxy-1-phenoxybenzeneHCID 68425585—

반응 단계

Under nitrogen, ZnCl2 (0.5 M solution in tetrahydrofuran; 6.8 mL, 3.41 mmol) was added by syringe to a round-bottomed flask sealed with a rubber septum and purged with nitrogen. Hexyl magnesium chloride (1.0 M solution in THF; 4.0 mL, 4.26 mmol) was then added dropwise by syringe, and the resulting solution was stirred at room temperature for 20 minutes. Next, N-methylpyrrolidinone (4.7 mL) was added by syringe. After 5 minutes, 21.7 mg (0.0426 mmol) Pd(P(t-Bu)3)2 and 500 mg (2.13 mmol) of compound (3) were added. The flask was then fitted with a reflux condenser and heated under refluxed for 48 hours. The flask was then gradually cooled to room temperature, and 20 mL of a 1.0M aqueous HCl solution was added. The resulting mixture was extracted with diethyl ether and the ether extract was washed with water, then dried over anhydrous MgSO4 and concentrated under vacuum to give the crude product. Purification by flash chromatography on silica gel afforded analytically pure compound (4a): 1H NMR (300 MHz) (CDCl3): δ 7.36-6.80 (m, 8H), 3.90 (s, 3H), 2.71-2.66 (t, 2H), 1.74-1.67 (m, 2H), 1.42-1.33 (m, 6H), 1.01-0.97 (t, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07687547B2
출처 데이터셋uspto-grants-2010_03
ORD IDord-12a50118fbf5444c8e6902f424180700
출처 메모uspto-grants-2010_03