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Hydrochloric Acid → HCID 20285690、化合物

HRID 904485
ノート
印刷プレビュー

反応式

HRID 904485 の反応式
[Cl:1][C:2]1[S:3][C:4]([Cl:8])=[CH:5][C:6]=1C.C=O.[ClH:11].CCO[CH2:15][CH3:16]>[Cl-].[Zn+2].[Cl-]>[Cl:11][CH2:6][C:5]1[C:15]([CH3:16])=[C:2]([Cl:1])[S:3][C:4]=1[Cl:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 712FormaldehydeHCID 3283Diethyl EtherHCID 2689102,5-Dichloro-3-methylthiophene

生成物 1

HCID 20285690HCID 20285690、化合物

試薬・触媒・溶媒 1

HCID 3007855Zincchloride触媒

実験手順

A mixture of 61.59 g. (0.368 mol) of 2,5-dichloro-3-methylthiophene, 13.1 g. of paraformaldehyde and 3.1 g. of zinc chloride was heated to 55° C. Hydrogen chloride gas was passed through the mixture for 7.25 hours. The resulting mixture was cooled and poured into a mixture of ether and ice water. The organic phase was separated and washed with sodium chloride solution, sodium bicarbonate solution and sodium chloride solution again. Evaporation of the dried solvent gave a dark brown oil which was distilled under reduced pressure to yield 3-chloromethyl-2,5-dichloro-4-methylthiophene as a pale yellow liquid, b.p. 87°-92° C./0.75 mm.

後処理

  1. additionA mixture of 61.59 g
  2. temperatureThe resulting mixture was cooled
  3. customThe organic phase was separated
  4. washwashed with sodium chloride solution, sodium bicarbonate solution and sodium chloride solution again
  5. customEvaporation of the dried solvent
  6. customgave a dark brown oil which
  7. distillationwas distilled under reduced pressure

出典と根拠

ORDレコード
ord-3332a3f3907047e8a93a2c81ae7cc26d
出典データセット
uspto-grants-1980_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04230872

反応ノート

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