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HRID 63321作成日:2026年10月23日

Potassium Carbonate → Cyclohexylmethyl 5-bromofuran-2-carboxylate

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

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物5-Bromo-2-furanecarboxylic acidHCID 68511—
反応物Cyclohexane, (bromomethyl)-HCID 137636—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物Cyclohexylmethyl 5-bromofuran-2-carboxylateHCID 86694615—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447078B2
出典データセットuspto-grants-2016_09
ORD IDord-49f17556297445d296f005a98aae47f5
出典メモuspto-grants-2016_09