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1-(3-Hydroxy-4-methoxyphenyl)ethanone → HCID 25100251、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-(3-Hydroxy-4-methoxyphenyl)ethanone | HCID 95693 | — |
| 反応物 | HCID 66761654 | HCID 66761654 | — |
| 生成物 | HCID 25100251 | HCID 25100251 | 91% |
反応手順
Acetophenone 12 (50 mg, 0.301 mmol) was condensed with O-(3-methylbenzyl)hydroxylamine hydrochloride (28) (57 mg, 0.328 mmol) according to the general procedure II-B defined above. After being heated for 15 h the reaction mixture was cooled and the solvent removed under reduced pressure. The ensuing residue was dissolved in CH2Cl2 (15 mL), washed with H2O (2×10 mL) then dried (MgSO4), filtered and concentrated under reduced pressure. The oil thus obtained was subjected to flash chromatography (1:19 v/v ethyl acetate/hexane elution) to afford the title compound CP30264 (78 mg, 91%) as a pale-orange oil, Rf 0.6 in 1:1 v/v ethyl acetate/hexane.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08536157B2 |
| 出典データセット | uspto-grants-2013_09 |
| ORD ID | ord-b6fa4720a0034f139aef0d71cd3f1cc4 |
| 出典メモ | uspto-grants-2013_09 |