Ammonia → 2,3-Dichloro-4,6-dinitrophenol

HRID 1609376ノート

反応式

HRID 1609376 の反応式
NC1C([OH:8])=CC(O)=C(N)C=1.[OH-].[Na+].N.[O-]O.C1(C(C)C)C=CC=CC=1.[Cl:25][C:26]1[CH:31]=[C:30]([N+:32]([O-:34])=[O:33])[CH:29]=[C:28]([N+:35]([O-:37])=[O:36])[C:27]=1[Cl:38]>C(Cl)Cl>[Cl:25][C:26]1[C:27]([Cl:38])=[C:28]([N+:35]([O-:37])=[O:36])[CH:29]=[C:30]([N+:32]([O-:34])=[O:33])[C:31]=1[OH:8]

参加物

7

反応物 5

HCID 222Ammonia4 回HCID 14798Sodium HydroxideHCID 4588214,6-DiaminoresorcinolHCID 110209011,2-Dichloro-3,5-dinitrobenzeneHCID 53627471Cumen hydroperoxide

生成物 1

HCID 108579782,3-Dichloro-4,6-dinitrophenol

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

In a preferred embodiment for making diaminoresorcinol, the base, e.g., sodium hydroxide, is first dissolved in refluxing liquid ammonia in an inert atmosphere. The temperature of refluxing liquid ammonia is dependent upon the pressure and is typically between about -50° C. to about -10° C. Under atmospheric pressure conditions, the refluxing temperature of liquid ammonia is about -33° C. A solution of cumene hydroperoxide and 1,2-dichloro-3,5-dinitrobenzene in methylene chloride is then added to the stirred liquid ammonia reaction mixture at a rate such that the temperature remains at the refluxing temperature. Upon completion of the addition, the ammonia is evaporated and 2,3-dichloro-4,6-dinitrophenol may be isolated by pouring the reaction mixture into excess aqueous hydrochloric acid and extracted with ethyl acetate. Preferably, the 2,3-dichloro-4,6-dinitrophenol product is not isolated or purified, but is directly converted to 4,6-diaminoresorcinol, thus making the production of 4,6-diaminoresorcinol from 1,2-dichloro-3,5-dinitrobenzene a "one pot" process.

後処理

  1. customis typically between about -50° C. to about -10° C
  2. customis about -33° C
  3. additionUpon completion of the addition
  4. customthe ammonia is evaporated

出典と根拠

ORDレコード
ord-429a71b20f00411088209a83430522f2
出典データセット
uspto-grants-1995_03
特許番号
US05399768

反応ノート

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