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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 472786생성일: 2026년 10월 26일

Dimethylformamide → Methyl 6-formyl-1-naphthoate

https://huagongshe.com/reaction/472786

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TriethylamineHCID 8471—
반응물1,3-Bis(diphenylphosphino)propaneHCID 81219—
반응물Trioctylsilane, 95%HCID 87780—
반응물Methyl 6-(((trifluoromethyl)sulfonyl)oxy)-1-naphthoateHCID 22622428—
반응물HCID 178418416HCID 178418416—
촉매palladium(II) acetateHCID 167845—
생성물Methyl 6-formyl-1-naphthoateHCID 5805697936%

반응 조건

온도70 °C

반응 단계

Carbon monoxide (CO) gas was slowly bubbled through a solution of methyl 6-(((trifluoromethyl)sulfonyl)oxy)-1-naphthoate (334 mg, 1.0 mmol), Pd(OAc)2 (22 mg, 0.10 mmol), 1,3-bis-(diphenylphosphino)propane (40 mg, 0.10 mmol) and triethylamine (0.28 mL, 2.0 mmol) an DMF (8.3 mL). After 15 min, trioctylsilane (0.90 mL, 2.0 mmol) was added as bubbling continued. The mixture was heated at 70° C., continuing to bubble CO into the solution. After 6 h at 70 the bubbling CO was replaced with a balloon of CO and the reaction mixture was stirred overnight. After 18 h at 70° C., the reaction was cooled to room temperature, diluted with EtOAc (150 mL) and washed with water (3×50 mL) and brine (50 mL). The organic phase was dried (Na2SO4), filtered and concentrated in vacuo. The resulting residue was purified on 40 g silica gel (100% hexanes→25% EtOAc/hexanes, gradient) to afford 78 mg (36%) of methyl 6-formyl-1-naphthoate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08633220B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-f1f9697f468c45b4bb16255818f39e02
출처 메모uspto-grants-2014_01