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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1080776Generated: October 25, 2026

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

https://huagongshe.com/reaction/1080776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl 4-(bromomethyl)-3-methoxybenzoateHCID 2759828—
Reactant5-Nitro-1-benzothiopheneHCID 12414084—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-methoxy4-(5-nitrobenzo[b]thien-3-ylmethyl)benzoateHCID 14763112—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05583152
Source datasetuspto-grants-1996_12
ORD IDord-2bc36345b6684ca1842f473286c5f136
Source noteuspto-grants-1996_12