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

HRID 260447노트

반응식

HRID 260447 반응식
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

참가 물질

7

반응물 3

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

생성물 1

HCID 233701944-(3-Furyl)-7-mercaptocoumarin수율 90.8%

시약·촉매·용매 3

HCID 962Water용매HCID 6228Dimethylformamide용매HCID 8028Tetrahydrofuran용매

실험 절차

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.

후처리

  1. filtrationfiltered

출처 및 근거

ORD 기록
ord-0f4377e8640246c0b12476d1fd85b086
출처 데이터셋
uspto-grants-1996_06
특허 번호
US05527827

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