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HRID 2217635作成日:2026年10月26日

Citric Acid → HCID 86589687、化合物

https://huagongshe.com/reaction/2217635

反応式

関与物質

役割名称HCID仕込み量
反応物Citric AcidHCID 311—
反応物(3,5-Dimethoxybenzyl)triphenylphosphonium bromideHCID 10962038—
反応物Potassium tert-butoxideHCID 23665647—
反応物4-[4-(2,4-Dioxothiazolidin-5-ylmethyl)-phenoxy]-benzaldehydeHCID 59768293—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 86589687HCID 86589687—

反応条件

温度0 °C

反応手順

To a suspension of 3,5-dimethoxybenzyltriphenylphosphonium bromide (0.82 g, 2.0 mmol) in THF (10 mL) at 0° C. was added solid potassium tert-butoxide (224 mg, 2.0 mmol). The resultant red solution was stirred for 15 min at 0° C. then cooled to −78° C. Solid 53 (0.3 mg, 0.90 mmol) was added and the reaction was allowed to warm to room temperature. After 30 min 10% citric acid (50 mL) was added and the mixture was partitioned between water (50 mL) and ethyl acetate (75 mL). The organic layer was washed with water (50 mL) and brine (50 mL) then dried (MgSO4), filtered and concentrated in vacuo. The crude product was purified by flash chromatography using hexanes-ethyl acetate (7:3) to yield 55 as a slightly opaque film (25 mg, 6%) after concentration and drying under high vacuum. 1H NMR (400 MHz, DMSO-d6): δ 12.04 (b s, 1H), 7.26 (d, J=8.8 Hz, 2H), 7.25 (d, J=8.8 Hz, 2H), 6.93 (d, J=8.4 Hz, 2H), 6.91 (d, J=8.4 Hz, 2H), 6.61 (d, J=12.4 Hz, 1H), 6.53 (d, J=12.0 Hz, 1H), 6.39 (d, J=2.4 Hz, 1H), 6.36 (t, J=2.4 Hz, 1H), 4.90 (dd, J=9.2 and 4.4 Hz, 1H), 3.62 (s, 6H), 3.36 (dd, J=14.0 and 4.4 Hz, 1H), 3.11 (dd, J=14.4, 8.8 Hz, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07407978B2
出典データセットuspto-grants-2008_08
ORD IDord-9fcb1e0df5cc4db589d0e5f590873e5e
出典メモuspto-grants-2008_08