Hydrochloric Acid → 4-(3-Furyl)-7-mercaptocoumarin

HRID 741833ノート

反応式

HRID 741833 の反応式
C[Si](C)(C)CC[S:5][C:6]1[CH:15]=[C:14]2[C:9]([C:10]([C:17]3[CH:21]=[CH:20][O:19][CH:18]=3)=[CH:11][C:12](=[O:16])[O:13]2)=[CH:8][CH:7]=1.[N+](CCCC)(CCCC)(CCCC)CCCC.[F-].Cl>CN(C=O)C.C1COCC1.O>[SH:5][C:6]1[CH:15]=[C:14]2[C:9]([C:10]([C:17]3[CH:21]=[CH:20][O:19][CH:18]=3)=[CH:11][C:12](=[O:16])[O:13]2)=[CH:8][CH:7]=1

参加物

7

反応物 3

HCID 313Hydrochloric AcidHCID 2724141Tetrabutylammonium FluorideHCID 233702447-(2-Trimethylsilylethylthio)-4-(3-furyl)coumarin

生成物 1

HCID 233701944-(3-Furyl)-7-mercaptocoumarin収率 90.8%

試薬・触媒・溶媒 3

HCID 962Water溶媒HCID 6228Dimethylformamide溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

The coumarin from Step 1 (963 mg) was dissolved in DMF (25 mL) and to this solution there was added n-Bu4NF (1M) in THF (8.4 mL). The mixture was stirred at r.t. for 2 h, poured onto 1N aqueous HCl (50 mL), diluted with H2O (50mL) and filtered to afford the title compound (620 mg) as a tan solid. m.p.: 167°-170° C.

後処理

  1. filtrationfiltered

出典と根拠

ORDレコード
ord-ea726db8bba4403781fcd7bc4c799aa0
出典データセット
uspto-grants-1996_09
特許番号
US05552437

反応ノート

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