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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 883827생성일: 2026년 10월 27일

Chromate → Bis(3,5-dimethoxyphenyl)methanone

https://huagongshe.com/reaction/883827

반응식

참여 물질

역할이름HCID투입량
반응물ChromateHCID 24461—
반응물Bis(3,5-dimethoxyphenyl)methanolHCID 67173126—
반응물HCID 178418287HCID 178418287—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
생성물Bis(3,5-dimethoxyphenyl)methanoneHCID 2160969263%

반응 단계

Pyridinium chlorochromate (PCC) (12.9 g, 30 mmol) was suspended in 30 mL dichloromethane in a 200 mL round bottom flask. Crude bis(3,5-dimethoxyphenyl)methanol from above (compound A) was suspended in 30 mL dichloromethane then added to the chromate suspension. The dark solution was allowed to stir at ambient temperature for 18 hours then diluted with ether. After decantation, the organic solution was washed twice with 1N NaOH, twice with 10% HCl, saturated NaHCO3, and then with brine. It was dried over anhydrous MgSO4, filtered and concentrated to give a brownish yellow solid. The brownish yellow solid was purified by column chromatography using 50% acetone/hexane as eluent giving the product as a yellow solid in 63% yield over 2 steps: IR (cm−1): 2960, 2938, 2834, 1660, 1592, 1456, 1425, 1349, 1304, 1205, 1157, 1066, 744; 1H NMR (250 MHz, C6D6): δ 3.21 (s, 12H), 6.67 (t, J=2.2 Hz, 2H), 7.21 (d, J=2.5 Hz, 4H); 13C NMR (63 MHz, C6D6): 54.9 (4C), 105.3 (2C), 108.0 (4C), 140.2 (2C), 161.1 (4C), 195.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08237003B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-911afee0ea70455fa675b44eb38baa0f
출처 메모uspto-grants-2012_08