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Ammonia → HCID 18783143、化合物

HRID 1420873
ノート
印刷プレビュー

反応式

HRID 1420873 の反応式
[CH3:1][C:2]1(O)[CH2:7][C:6]([CH3:9])([CH3:8])[CH2:5][C:4]([CH3:11])([CH3:10])[CH2:3]1.[OH2:13].N.[C:15](#[N:17])[CH3:16]>>[C:15]([NH:17][C:2]1([CH3:1])[CH2:7][C:6]([CH3:9])([CH3:8])[CH2:5][C:4]([CH3:11])([CH3:10])[CH2:3]1)(=[O:13])[CH3:16]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 222AmmoniaHCID 962WaterHCID 6342AcetonitrileHCID 1422881,3,3,5,5-Pentamethylcyclohexanol

生成物 1

HCID 18783143HCID 18783143、化合物収率 60%

反応条件

温度
-50 °C

実験手順

To a vigorously stirred solution of 1,3,3,5,5-pentamethylcyclohexanol (3-13) (3.0 g, 17.65 mmol) in acetonitrile (20 ml) fuming HNO3 (6ml) was added dropwise, keeping temperature below 45° C. The resulting mixture was stirred at -50° C. for 6 h, then it was cooled, poured into water (30 ml) ana neutralised with aqueous NH3. Aqueous phase was extracted with ether (3*30 ml). The combined ether phases were washed with saline (30 ml), then dried over MgSO4, filtered and evaporated. The crude product was crystallised from cold acetonitrile to give 223 g (60%) of 14-2 as a white crystals, m.p. 110° C.

後処理

  1. customtemperature below 45° C
  2. temperatureit was cooled
  3. extractionAqueous phase was extracted with ether (3*30 ml)
  4. washThe combined ether phases were washed with saline (30 ml)
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. customevaporated
  8. customThe crude product was crystallised from cold acetonitrile

出典と根拠

ORDレコード
ord-11ed142ceef94d2e99b3f55577bf2078
出典データセット
uspto-grants-2000_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06071966

反応ノート

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