Tetrahydrofuran → Methyl 2-(2-formyl-4-ethylphenoxy)propionate

HRID 482436

反応式

HRID 482436 の反応式
C([C:3]1[CH:4]=[C:5]([OH:11])[C:6](=[CH:9][CH:10]=1)[CH:7]=[O:8])C.Br[CH:13]([CH3:18])[C:14]([O:16][CH3:17])=[O:15].C(=O)([O-])[O-].[K+].[K+].O1CC[CH2:27][CH2:26]1>>[CH:7]([C:6]1[CH:9]=[C:10]([CH2:26][CH3:27])[CH:3]=[CH:4][C:5]=1[O:11][CH:13]([CH3:18])[C:14]([O:16][CH3:17])=[O:15])=[O:8]

参加物

5

実験手順

By the method of Example 1, Step F, 32.33 grams (0.215 mole) of 4-ethylsalicylaldehyde and 35.9 grams (0.215 mole) of methyl 2-bromopropionate was reacted in the presence of 35.7 grams (0.258 mole) of potassium carbonate in 50 mL of tetrahydrofuran, yielding 49.16 grams of methyl 2-(2-formyl-4-ethylphenoxy)propionate. The NMR spectrum was consistent with the proposed spectrum.

出典と根拠

ORDレコード
ord-a38643e302ce4e87917a8e37b9e017fe
出典データセット
uspto-grants-1998_08
特許番号
US05798316

関連ノート

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