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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408795Generated: October 31, 2026

Benzyl mercaptan → 4-Benzylsulfanyl-5-nitro-thiophene-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2408795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl mercaptanHCID 7509—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-5-nitro-thiophene-3-carboxylic acid ethyl esterHCID 57455183—
SolventEthanolHCID 702—
Product4-Benzylsulfanyl-5-nitro-thiophene-3-carboxylic acid ethyl esterHCID 5745518498%

Reaction Conditions

Temperature25 °C

Reaction Steps

An aqueous solution of potassium carbonate (9.90 g, 71.6 mmol, dissolved in 40 mL water) was added to a suspension of 4-bromo-5-nitro-thiophene-3-carboxylic acid ethyl ester (20.06 g, 71.6 mmol) in ethanol at 25° C. Benzyl mercaptan (8.41 mL, 71.6 mmol) was added via pipette, and the dark red reaction mixture was stirred at 25° C. for 4 h and then was concentrated in vacuo to near-dryness. The remaining orange-brown solid was triturated with water (200 mL) and was collected by filtration. After washing with water (200 mL), the resulting solid was air-dried overnight to afford the desired product, 4-benzylsulfanyl-5-nitro-thiophene-3-carboxylic acid ethyl ester (22.63 g, 70.0 mmol, 98%), as a yellow/brown solid. 1H NMR (400 MHz, CDCl3) δ: 1.41 (3H, t, J=7.1 Hz), 4.25 (2H, s), 4.39 (2H, q, J=7.0 Hz), 7.18-7.23 (5H, m), 8.07 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815847B2
Source datasetuspto-grants-2014_08
ORD IDord-ff5c82a81b72423cbbc610f4dcf72f62
Source noteuspto-grants-2014_08