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HRID 1670428作成日:2026年10月27日

Vinylcyclopentane → (3R,4R,5S)-5-[(1R,2E)-3-cyclopentyl-1-hydroxyprop-2-en-1-yl]-4-hydroxy-3-methoxydihydrofuran-2(3H)-one

https://huagongshe.com/reaction/1670428

反応式

関与物質

役割名称HCID仕込み量
反応物VinylcyclopentaneHCID 77345—
反応物(3R,4R,5S)-4-hydroxy-5-[(1R)-1-hydroxyprop-2-en-1-yl]-3-methoxydihydrofuran-2(3H)-oneHCID 67241097—
触媒HCID 178479819HCID 178479819—
溶媒DichloromethaneHCID 6344—
生成物(3R,4R,5S)-5-[(1R,2E)-3-cyclopentyl-1-hydroxyprop-2-en-1-yl]-4-hydroxy-3-methoxydihydrofuran-2(3H)-oneHCID 5746378451%

反応手順

2 g of 31 (10.63 mmol), 4.22 g of vinylcyclopentane (43.92 mmol), 80 mL of CH2Cl2 and 226 mg of 2nd generation Grubb's catalyst (C46H65Cl2N2PRu, MW 848.98, 0.266 mmol) are added to a 250 mL round-bottomed flask. The medium is stirred for 2 h at RT and then heated for 4 h at 45° C. The insoluble material is filtered and then the solvent is evaporated and the crude product (3.39 g) is chromatographed on a silica cartridge (150 g), eluting with a heptane/AcOEt (50/50) mixture. 1.39 g of expected product 32 (white solid) are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07994161B2
出典データセットuspto-grants-2011_08
ORD IDord-051f1945619d4cfcb76a808bc8be29b8
出典メモuspto-grants-2011_08