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4-Toluenesulfonyl chloride → HCID 3296813、化合物

HRID 2294762
ノート
印刷プレビュー

反応式

HRID 2294762 の反応式
[N-]=[N+:2]=[N-:3].[Na+].C1(C)C=CC(S(Cl)(=O)=O)=CC=1.[C:16]([O:24][CH2:25][CH3:26])(=[O:23])[CH2:17][C:18]([O:20][CH2:21][CH3:22])=[O:19].C(N(CC)CC)C>O.C(O)C>[N+:2](=[C:17]([C:18]([O:20][CH2:21][CH3:22])=[O:19])[C:16]([O:24][CH2:25][CH3:26])=[O:23])=[N-:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 73974-Toluenesulfonyl chlorideHCID 7761Diethyl MalonateHCID 8471TriethylamineHCID 33557Sodium Azide

生成物 1

HCID 3296813HCID 3296813、化合物収率 88.6%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒
HCID 962
Water
溶媒

実験手順

A mixture of sodium azide (683 mg, 10.5 mmol), p-toluenesulfonyl chloride (2.0 grams, 10.5 mmol), and 70% aqueous ethanol (30 mL) was stirred at room temperature for 1 hour. Diethyl malonate (1.62 mL, 10.0 mmol) and triethylamine (1.46 mL, 10.5 mmol) were added. The reaction mixture was stirred at room temperature for 1.5 hours and then poured into deionized water (200 mL). The mixture was extracted with petroleum ether. The extracts were combined and decanted from the solid that formed. The petroleum ether solution was washed with a saturated aqueous sodium chloride solution. The organic solution was dried using anhydrous magnesium sulfate, filtered, and concentrated to give 1.65 grams of diethyl 2-diazomalonate as a yellow oil. IR (KBr): 2138, 1757, 1735, 1320, 1092 cm-1. Decomposition temperature: 175° C. (by DSC).

後処理

  1. stirringThe reaction mixture was stirred at room temperature for 1.5 hours
  2. extractionThe mixture was extracted with petroleum ether
  3. customdecanted from the solid
  4. customthat formed
  5. washThe petroleum ether solution was washed with a saturated aqueous sodium chloride solution
  6. customThe organic solution was dried
  7. filtrationfiltered
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-259ec1b3244a488292360c6ca67d68ba
出典データセット
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05691098

反応ノート

読み込み中…

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