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HRID 921129作成日:2026年10月27日

Triphenylphosphine → (S)-4,5-difluoro-2-(pent-4-en-2-yloxy)benzaldehyde

https://huagongshe.com/reaction/921129

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Diisopropyl azodicarboxylateHCID 5363146—
反応物(2R)-pent-4-en-2-olHCID 6999724—
反応物4,5-Difluoro-2-hydroxybenzaldehydeHCID 15434553—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物(S)-4,5-difluoro-2-(pent-4-en-2-yloxy)benzaldehydeHCID 1183070189.05%

反応手順

To a solution of 4,5-difluoro-2-hydroxybenzaldehyde (1.0 g, 6.33 mmol) in THF (14 ml) were added (R)-(−)-pent-4-en-2-ol (1.090 g, 12.65 mmol) and triphenylphosphine (2.157 g, 8.22 mmol). DIAD (1.599 ml, 8.22 mmol) was added dropwise (exotherm) and the mixture was stirred at rt. After 1.5 h, the mixture was diluted with Et2O and washed with 1N NaOH followed by water (3×'s) then brine, dried (Na2SO4), filtered and concentrated. The yellow oil was purified by flash chromatography (Biotage; 0%-100% EtOAc/hexane; 20 CV) to give (S)-4,5-difluoro-2-(pent-4-en-2-yloxy)benzaldehyde (0.1295 g, 0.572 mmol, 9.05% yield) as a yellow oil. 1H NMR (400 MHz, CDCl3) δ 10.36 (d, J=3.2 Hz, 1H), 7.76-7.55 (m, 1H), 6.83 (dd, J=11.9, 6.0 Hz, 1H), 6.04-5.67 (m, 1H), 5.23-5.06 (m, 2H), 4.48 (sxt, J=6.0 Hz, 1H), 2.71-2.35 (m, 2H), 1.41 (d, J=6.1 Hz, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09273067B2
出典データセットuspto-grants-2016_03
ORD IDord-4b29f591b603425e81dc27f63be7a1ef
出典メモuspto-grants-2016_03