Oxalyl chloride → 2-Furansulfonyl isocyanate

HRID 27346

反応式

HRID 27346 の反応式
C(Cl)(=O)[C:2](Cl)=[O:3].N12CCC(CC1)CN2.[O:15]1[CH:19]=[CH:18][CH:17]=[C:16]1[S:20]([NH2:23])(=[O:22])=[O:21]>C1(C)C=CC=CC=1>[O:15]1[CH:19]=[CH:18][CH:17]=[C:16]1[S:20]([N:23]=[C:2]=[O:3])(=[O:22])=[O:21]

参加物

5

反応物 3

HCID 65578Oxalyl chlorideHCID 136165Diazabicyclo(2.2.2)octaneHCID 13668256Furan-2-sulfonamide

生成物 1

HCID 233424782-Furansulfonyl isocyanate

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

Dry toluene (150 ml), 25 ml of oxalyl chloride (295), and a trace of DABCO (diaza-bicyclo[2.2.2]octane) were heated to 90°. Ten g of 2-furansulfonamide was added over a 15 minute period and the mixture was held at 95° for 2 hours. After filtering, the solvent was removed under vacuum to yield 2.1 g of an oil showing the characteristic isocyanate absorption in the infrared (2280 cm-1).

後処理

  1. filtrationAfter filtering
  2. customthe solvent was removed under vacuum

出典と根拠

ORDレコード
ord-989e8416a8634b9e8cbdc96eb0350707
出典データセット
uspto-grants-1980_09
特許番号
US04221585

関連ノート

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