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HRID 5559作成日:2026年10月24日

Hydrochloric Acid → (S)-1-(2-Furyl)-1-pentanol

https://huagongshe.com/ja/reaction/5559

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物2-PentanoylfuranHCID 231325—
反応物DiboronHCID 6328200—
反応物[1,3,2] OxazaboroleHCID 18375910—
溶媒MethanolHCID 887—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物(S)-1-(2-Furyl)-1-pentanolHCID 5432436170%

反応条件

温度10 °C

反応手順

10.4 mmol (10.4 mL) of diborane (1 M solution in THF) was added dropwise in a period of 10 m at room temperature to a solution of 2-valeryl furan (2.62 g, 17.2 mmol) and 1.68 mmol (4.2 mL) of (3aR)-1,3,3-triphenyl pyrrolidino [1,2-c] [1,3,2] oxazaborole (see E. J. Corey et al. J. Am. Chem. Soc. 1987, 109, 7925-26, 0.4M solution in THF) in 25 mL THF. The reaction mixture was stirred for 20 m and was cooled to 10° C. 6 mL methanol was cautiously added and followed by adding 62 mg HCl (by weight) in ether. Stirred for 0.5 h, white solid was precipitated out. The cloudy mixture was poured into 100 mL ether and 100 mL water. The organic layer was separated, washed with saturated sodium bicarbonate, water, brine, dried and filtered. The filtrate was evaporated to an yellowish oil which was chromatographed eluting with 10 % ethyl acetate in hexane to obtain 70% of the product. [α]25D =-13°, 60% ee by Mosher' ester analysis.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05244910
出典データセットuspto-grants-1993_09
ORD IDord-c3362f70087947e9a7caa72bda54863b
出典メモuspto-grants-1993_09