HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421447Generated: November 1, 2026
Benzyl mercaptan → 4-Benzylsulfanyl-5-nitro-thiophene-3-carboxylic acid ethyl ester
https://huagongshe.com/reaction/421447
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-5-nitro-thiophene-3-carboxylic acid ethyl ester | HCID 57455183 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Benzylsulfanyl-5-nitro-thiophene-3-carboxylic acid ethyl ester | HCID 57455184 | 98% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08097613B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-10f3b48ea8394c78808b4d0e231711a9 |
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| Source note | uspto-grants-2012_01 |
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