Chloroacetyl chloride → Ethyl 2-(chloromethyl)-1,3-benzoxazole-5-carboxylate

HRID 465046Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 465046
[OH:1][C:2]1[CH:12]=[CH:11][C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:4][C:3]=1[N+:13]([O-])=O.[Cl:16][CH2:17][C:18](Cl)=O.P(Cl)(Cl)(Cl)=O>[Ni].C(O)C>[Cl:16][CH2:17][C:18]1[O:1][C:2]2[CH:12]=[CH:11][C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:4][C:3]=2[N:13]=1

Komponenten

6

Edukt 3

HCID 6577Chloroacetyl chlorideHCID 24813Phosphorus oxychlorideHCID 87895Benzoic acid, 4-hydroxy-3-nitro-, ethyl ester

Produkt 1

HCID 15211498Ethyl 2-(chloromethyl)-1,3-benzoxazole-5-carboxylate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 935NickelKatalysatorHCID 702EthanolLösungsmittel

Versuchsvorschrift

Ethyl 4-hydroxy-3-nitrobenzoate (32 g) prepared according to the method described in J. Org. Chem., vol. 26, p. 2223 (1961) was subjected to reduction under increased pressure at 70 atm in the presence of a Raney Nickel catalyst in absolute ethanol (200 ml). The product was then caused to react with chloroacetyl chloride, and was subsequently subjected to ring closure with phosphorous oxychloride to yield 2-chloromethyl-5-ethoxycarbonylbenzoxazole (27.3 g). The chloromethyl compound (10 g) was caused to react with dimethylamine to yield 2-dimethylaminomethyl-5-ethoxycarbonylbenzoxazole (6 g), which was subsequently subjected to reduction with lithium aluminium hydride in anhydrous tetrahydrofuran (60 ml) thereby to obtain 2-dimethylaminomethyl-5-hydroxymethylbenzoxazole (2 g).

Quellen und Nachweise

ORD-Eintrag
ord-f637b528364845b0bd11923a64889953
Quelldatensatz
uspto-grants-1985_10
Patentnummer
US04550118

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