Phenothiazine → 5-Acryloyloxymethyl-oxazolidin-2-one

HRID 726488

反応式

HRID 726488 の反応式
[OH:1][CH2:2][CH:3]1[O:7][C:6](=[O:8])[NH:5][CH2:4]1.C(N(CC)CC)C.C1C2NC3C(=CC=CC=3)SC=2C=CC=1.[C:30](Cl)(=[O:33])[CH:31]=[CH2:32]>O1CCCC1>[C:30]([O:1][CH2:2][CH:3]1[O:7][C:6](=[O:8])[NH:5][CH2:4]1)(=[O:33])[CH:31]=[CH2:32]

参加物

6

実験手順

105 g (0.90 mol.) of 5-hydroxymethyl-oxazolidin-2-one were placed into a one liter, three necked, round bottomed flask equipped with a paddle stirrer and thermometer. This was followed by 500 ml of tetrahydrofuran, 101 g (1.0 mol.) of triethylamine and 0.5 g of phenothiazine. Stirring was started as 90 g (1.0 mol.) of acryloyl chloride were added dropwise in such a way that the contents of the flask were maintained at 30° C. or less. When the addition was complete, the contents were stirred overnight at room temperature. The triethylamine hydrochloride was filtered and the solution was allowed to stand over NaHCO3 and Na2SO4. The solution was filtered, transferred to a one liter, round bottomed flask and placed on a rotoevaporator. The solution was concentrated by purging with a stream of air while rotating the flask. The resulting liquid was confirmed by 13C NMR to contain a mixture of the desired product and unreacted starting material.

後処理

  1. customround bottomed flask equipped with a paddle stirrer
  2. additionwere added dropwise in such a way that the contents of the flask
  3. temperaturewere maintained at 30° C. or less
  4. additionWhen the addition
  5. stirringthe contents were stirred overnight at room temperature
  6. filtrationThe triethylamine hydrochloride was filtered
  7. filtrationThe solution was filtered
  8. concentrationThe solution was concentrated
  9. customby purging with a stream of air
  10. additiona mixture of the desired product

出典と根拠

ORDレコード
ord-393f3dc0592243789d53d315f1349fe9
出典データセット
uspto-grants-1998_01
特許番号
US05709935

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