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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 63321생성일: 2026년 10월 23일

Potassium Carbonate → Cyclohexylmethyl 5-bromofuran-2-carboxylate

https://huagongshe.com/ko/reaction/63321

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물5-Bromo-2-furanecarboxylic acidHCID 68511—
반응물Cyclohexane, (bromomethyl)-HCID 137636—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물Cyclohexylmethyl 5-bromofuran-2-carboxylateHCID 86694615—

반응 단계

A mixture of 5-bromofuran-2-carboxylic acid (2.64 g, 13.8 mmol), (cyclohexylmethyl)bromide (2.62 g, 14.8 mmol), K2CO3 (2.30 g, 16.64 mmol) in anhydrous NMP was stirred under Ar at +70° C. for 8 hrs after which additional (cyclohexylmethyl)bromide (1.55 g, 8.75 mmol) was added. Stirring continued overnight then the reaction mixture was concentrated under reduced pressure. The residue was partitioned between aqueous NaHCO3 (10%) and hexanes, and then aqueous layer was extracted with hexanes. Combined organic layers were washed with brine, dried over anhydrous MgSO4 and concentrated under reduced pressure to give cyclohexylmethyl 5-bromofuran-2-carboxylate as a light yellow oil. Yield (2.22 g, 56%); 1H NMR (400 MHz, CDCl3) δ 7.10 (d, J=3.9 Hz, 1H), 6.44 (d, J=3.4 Hz, 1H), 4.10 (d, J=6.4 Hz, 2H), 1.64-1.84 (m, 6H), 1.12-1.34 (m, 3H), 0.95-1.09 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447078B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-49f17556297445d296f005a98aae47f5
출처 메모uspto-grants-2016_09