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HRID 275135Erstellt: 26. Oktober 2026

Water → Methyl 3-methoxy4-(5-nitrobenzo[b]thien-3-ylmethyl)benzoate

https://huagongshe.com/reaction/275135

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktMethyl 4-(bromomethyl)-3-methoxybenzoateHCID 2759828—
Edukt5-Nitro-1-benzothiopheneHCID 12414084—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 3-methoxy4-(5-nitrobenzo[b]thien-3-ylmethyl)benzoateHCID 14763112—

Reaktionsschritte

Stannic chloride (0.41 g.) was added to a stirred solution of 5-nitrobenzo[b]thiophene (0.28 g.) and methyl 4-bromomethyl-3-methoxybenzoate (B) (0.61 g.) in dichloromethane (5 ml.). The mixture was heated under reflux for 18 hours. The cooled mixture was poured into water (10 ml.) and extracted with dichloromethane (2×20 ml.). The combined extracts were dried (MgSO4) and evaporated. The oil was purified by flash chromatography on silica gel (100 ml.) eluting with 1:9 v/v ethyl acetate:hexane. The solid obtained was crystallized from hexane to give methyl 3-methoxy-4-(5-nitrobenzo[b]thien-3-ylmethyl)benzoate (I) as a solid (0.16 g., 30%); NMR: (250 MHz, CDCl3): 3.92(s, 3H, OCH3), 3.98(s,3H, OCH3), 4.28(s,2H, CH2 --Ar), 7.15 (d,1H), 7.22(s,1H), 7.56(m,2H), 7.93(d,1H), 8.19(dd, 1H); 8.73(d,1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05391758
Quelldatensatzuspto-grants-1995_02
ORD IDord-369a7bbec6e046beb4ca9cbf490165aa
Quellennotizuspto-grants-1995_02