Thiazolidinedione → 5-[3-(Phenylmethoxy)phenylmethyl-ene]-2,4-thiazolidinedione

HRID 1728320ノート

反応式

HRID 1728320 の反応式
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH:14]=[CH:15][CH:16]=1)[CH:12]=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[S:17]1[CH2:21][C:20](=[O:22])[NH:19][C:18]1=[O:23].N1CCCCC1>N1C=CC=CC=1>[C:2]1([CH2:1][O:8][C:9]2[CH:10]=[C:11]([CH:12]=[C:21]3[S:17][C:18](=[O:23])[NH:19][C:20]3=[O:22])[CH:14]=[CH:15][CH:16]=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

5

反応物 3

HCID 5437ThiazolidinedioneHCID 8082PiperidineHCID 743423-Benzyloxybenzaldehyde

生成物 1

HCID 12494175-[3-(Phenylmethoxy)phenylmethyl-ene]-2,4-thiazolidinedione収率 100%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

A solution of 3-benzyloxybenzaldehyde (42.45 g, 200 mmol), 2,4-thiazolidinedione (23.43 g, 200.0 mmol), and piperidine (2 g) in 150 ml pyridine was refluxed for 16 h. The mixture was concentrated in vacuo, and the residue was triturated with 500 ml hot benzene, filtered, and the filtrate left standing at room temperature for two days. The resulting crystals were collected by filtration, washed with petroleum ether, and dried to give the product in 100% yield; mp 233-235° C.; IR (nujol): 1741, 1688 (CO) cm-1 ; NMR (DMSOd6TMS): δ5.19 (s, 2H, ArCH2), 7.15-7.25 (m, 3H), 7.3-7.5 (m, 6H), 7.73 (s, 1H, C=CH); Anal calcd for C17H13NO3, MW 311.36: C, 65.58; H, 4.21; N, 4.50; S, 10.30. Found: C, 65.53; H, 3.91; N, 4.52; S, 10.30. Mass spec m/e 312(M+1).

後処理

  1. concentrationThe mixture was concentrated in vacuo
  2. customthe residue was triturated with 500 ml hot benzene
  3. filtrationfiltered
  4. waitthe filtrate left
  5. filtrationThe resulting crystals were collected by filtration
  6. washwashed with petroleum ether
  7. customdried
  8. customto give the product in 100% yield

出典と根拠

ORDレコード
ord-b07df93b035f47fb8f7171a8c9c1051f
出典データセット
uspto-grants-1994_07
特許番号
US05326770

反応ノート

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