Dichloromethane methanol → 2,6-Dichloro-5-methoxypyrimidine-4-carbaldehyde

HRID 516536

反応式

HRID 516536 の反応式
[Cl:1][C:2]1[N:7]=[C:6]([CH:8]=C)[C:5]([O:10][CH3:11])=[C:4]([Cl:12])[N:3]=1.ClCCl.C[OH:17]>>[Cl:1][C:2]1[N:7]=[C:6]([CH:8]=[O:17])[C:5]([O:10][CH3:11])=[C:4]([Cl:12])[N:3]=1

参加物

3

反応物 2

HCID 21226129Dichloromethane methanolHCID 866893262,4-Dichloro-5-methoxy-6-vinylpyrimidine

生成物 1

HCID 866893302,6-Dichloro-5-methoxypyrimidine-4-carbaldehyde収率 100%

実験手順

A solution of 2,6-dichloro-5-methoxy-4-vinyl pyrimidine (50 g, 0.24 mol) in dichloromethane:methanol (4:1, 2 L) was cooled to −78° C. Ozone gas was bubbled through for 5 h. The reaction was quenched with dimethyl sulfide (50 mL). The mixture was slowly warmed to room temperature and concentrated under reduced pressure at 40° C. to provide the title compound (50.5 g, 100%).

後処理

  1. customOzone gas was bubbled through for 5 h
  2. customThe reaction was quenched with dimethyl sulfide (50 mL)
  3. concentrationconcentrated under reduced pressure at 40° C.

出典と根拠

ORDレコード
ord-97807976bb034a4cb515558593fe9c04
出典データセット
uspto-grants-2015_08
特許番号
US09113629B2

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