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HRID 931429생성일: 2026년 10월 26일

Sodium Carbonate → Methyl 4-(4-{[(4-tert-Butylphenyl)sulfonyl]methyl}-5-methyl-1,3-oxazol-2-yl)benzoate

https://huagongshe.com/reaction/931429

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참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물Sodium SulfiteHCID 24437—
반응물4-t-Butylbenzenesulfonyl chlorideHCID 139882—
반응물Methyl 4-(4-(chloromethyl)-5-methyloxazol-2-yl)benzoateHCID 23076573—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물Methyl 4-(4-{[(4-tert-Butylphenyl)sulfonyl]methyl}-5-methyl-1,3-oxazol-2-yl)benzoateHCID 6827831726.2%

반응 조건

온도100 °C

반응 단계

A solution of Na2SO3 (126 mg, 1.0 mmol) and Na2CO3 (106 mg, 1.0 mmol) in water (2 mL) was added to a suspension of 4-tert-butylbenzenesulfonyl chloride (233 mg, 1.0 mmol) in water (5 mL) and the mixture was stirred at 100° C. for 2 h. A solution of chloride 2 (268 mg, 1.0 mmol) in EtOH (5 mL) was added and the mixture stirred at 100° C. for 16 h. The mixture was cooled and diluted with water (40 mL) and stirred for 15 min. The precipitate was filtered, washed with water (5 mL). The residue purified by column chromatography, eluting with a gradient (20-50%) of EtOAc/pet. ether, to give benzoate 22 (112 mg, 26%) as a white powder: mp (EtOAc) 190-192° C.; 1H NMR (CDCl3) δ 8.05 (ddd, J=8.6, 1.8, 1.5 Hz, 2H, H-2, H-6), 7.89 (ddd, J=8.6, 1.8, 1.5 Hz, 2H, H-3, H-5), 7.71 (ddd, J=8.6, 2.2, 1.8 Hz, 2H, H-2′, H-6′), 7.51 (ddd, J=8.6, 2.2, 1.8 Hz, 2H, H-3′, H-5′), 4.30 (s, 2H, CH2SO2), 3.94 (s, 3H, OCH3), 2.32 (s, 3H, CH3), 1.33 [s, 9H, C(CH3)3]; MS m/z 428.5 (MH+, 100%). Anal. calcd for C23H25NO5S: C, 64.62; H, 5.89; N, 3.28. Found: C, 64.70; H, 5.94; N, 3.25%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09296732B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-bb13505d50a347c89092de3c8ac76ee7
출처 메모uspto-grants-2016_03