3-(4-Nitrobenzyl)-thiazolidine → 3-(4-Aminobenzyl)-thiazolidine

HRID 2373757ノート

反応式

HRID 2373757 の反応式
[N+:1]([C:4]1[CH:15]=[CH:14][C:7]([CH2:8][N:9]2[CH2:13][CH2:12][S:11][CH2:10]2)=[CH:6][CH:5]=1)([O-])=O>Cl>[NH2:1][C:4]1[CH:15]=[CH:14][C:7]([CH2:8][N:9]2[CH2:13][CH2:12][S:11][CH2:10]2)=[CH:6][CH:5]=1

参加物

3

反応物 1

HCID 219186763-(4-Nitrobenzyl)-thiazolidine

生成物 1

HCID 154105273-(4-Aminobenzyl)-thiazolidine収率 63%

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid溶媒

実験手順

3-(4-nitrobenzyl)-thiazolidine (1.1 g, 5 mmoles) is put into solution in 10 ml concentrated hydrochloric acid at 0° C. Dihydrated tin chloride (7.7 g, 34 mmoles) is added in portions, the mixture is heated for 2 hours under reflux and the acid is evaporated off under reduced pressure. The residue is then taken up in 20 ml of water and neutralized with a 2N soda solution (approximately 100 ml). 100 ml of dichloromethane is added to the medium and the whole is filtered on celite in order to eliminate the salts in suspension. The organic phase is extracted, washed 3 times with 50 ml of water, dried, filtered and evaporated to dryness under reduced pressure. The expected product is purified on silica gel in a dichloromethane/methanol (98/2) mixture and is obtained in the form of of a beige powder (0.6 g, 63%). Melting point: 73-74° C.

後処理

  1. temperaturethe mixture is heated for 2 hours
  2. temperatureunder reflux
  3. customthe acid is evaporated off under reduced pressure
  4. addition100 ml of dichloromethane is added to the medium
  5. filtrationthe whole is filtered on celite in order
  6. extractionThe organic phase is extracted
  7. washwashed 3 times with 50 ml of water
  8. customdried
  9. filtrationfiltered
  10. customevaporated to dryness under reduced pressure
  11. customThe expected product is purified on silica gel in a dichloromethane/methanol (98/2) mixture

出典と根拠

ORDレコード
ord-9255f81437d0495aaa9c54debeafc0fe
出典データセット
uspto-grants-2008_12
特許番号
US07459558B2

反応ノート

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