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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275136Generated: October 27, 2026

Sodium Bicarbonate → Methyl 4-(5-aminobenzo[b]thien-3-ylmethyl)-3-methoxybenzoate

https://huagongshe.com/reaction/275136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 3-methoxy4-(5-nitrobenzo[b]thien-3-ylmethyl)benzoateHCID 14763112—
SolventEthanolHCID 702—
ProductMethyl 4-(5-aminobenzo[b]thien-3-ylmethyl)-3-methoxybenzoateHCID 1476311354.6%

Reaction Steps

Stannous chloride dihydrate (0.38 g.) was added to a stirred solution of (I) (0.12 g.) in ethanol (5 ml.), under an atmosphere of nitrogen. The mixture was heated under reflux for 2 hours. The cooled mixture was basified with saturated aqueous sodium bicarbonate (15 ml.) and extracted with ethyl acetate (2×25 ml.). The extracts were dried (MgSO4) and evaporated. The residual oil was purified by flash chromatography on silica gel (50 ml.), eluting with 3:7 v/v ethyl acetate:hexane to give methyl 4-(5-aminobenzo[b]thien-3-ylmethyl)-3-methoxybenzoate (H) (0.06 g., 54 % ) as an oil; NMR (80 MHz, DMSO-d6): 3.84 (s,3H, OCH3), 3.91(s,3H, OCH3), 4.03(s,2H, CH2 --Ar), 5.0(br s,2H, NH2), 6.80(m,2H), 7.14(m,2H), 7.52(m,3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05391758
Source datasetuspto-grants-1995_02
ORD IDord-c719ec7a090d4b41a9624f6741acdd07
Source noteuspto-grants-1995_02