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Tetrabutylammonium Fluoride → 2-Cyano-4-(3-furyl)-7-mercaptonaphthalene

HRID 741836
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인쇄 미리보기

반응식

HRID 741836 반응식
[C:1]([C:3]1[CH:4]=[C:5]([C:20]2[CH:24]=[CH:23][O:22][CH:21]=2)[C:6]2[C:11]([CH:12]=1)=[CH:10][C:9]([S:13]CC[Si](C)(C)C)=[CH:8][CH:7]=2)#[N:2].[N+](CCCC)(CCCC)(CCCC)CCCC.[F-]>CN(C=O)C.C1COCC1.Cl>[C:1]([C:3]1[CH:4]=[C:5]([C:20]2[CH:24]=[CH:23][O:22][CH:21]=2)[C:6]2[C:11]([CH:12]=1)=[CH:10][C:9]([SH:13])=[CH:8][CH:7]=2)#[N:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 2724141Tetrabutylammonium FluorideHCID 194269713-Cyano-1-(furan-3-yl)-6-[2-trimethylsilylethylthio]naphthalene

생성물 1

HCID 233702312-Cyano-4-(3-furyl)-7-mercaptonaphthalene수율 82.4%

시약·촉매·용매 3

HCID 313Hydrochloric Acid용매HCID 6228Dimethylformamide용매HCID 8028Tetrahydrofuran용매

실험 절차

The product from Step 1 (1.8 g) was dissolved in DMF (40 mL) and there was added n-Bu4NF (1M) in THF (15 mL). The resulting mixture was stirred at r.t. for 1.5 h, diluted with 1N aqueous HCl (40 mL) then H2O (300 mL) and filtered to afford the title thiol (1.06 g) as a light orange solid m.p.: 144°-146° C.

후처리

  1. filtrationH2O (300 mL) and filtered

출처 및 근거

ORD 기록
ord-a737a7ab637e4d72a3fcf62e015646b0
출처 데이터셋
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05552437

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