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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646348Generated: October 30, 2026

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

https://huagongshe.com/reaction/1646348

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, 3 H, OCH3), 3.98 (s,3 H, OCH3), 4.28 (s,2 H, CH2 --Ar), 7.15 (d,1 H), 7.22 (s,1 H), 7.56 (m,2 H), 7.93 (d,1 H), 8.19 (dd, 1 H): 8.73 (d,1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05179112
Source datasetuspto-grants-1993_01
ORD IDord-07ffe88c78794048b6a7e5c1b9c1fed2
Source noteuspto-grants-1993_01