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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275135Generated: October 25, 2026

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

https://huagongshe.com/reaction/275135

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 numberUS05391758
Source datasetuspto-grants-1995_02
ORD IDord-369a7bbec6e046beb4ca9cbf490165aa
Source noteuspto-grants-1995_02