HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640347Generated: October 28, 2026
Acetic Acid → 2-(4-Methyl-benzyl)-5-(2-nitro-ethyl)-thiophene
https://huagongshe.com/reaction/640347
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(4-Methyl-benzyl)-5-((E)-2-nitro-vinyl)-thiophene | HCID 59255318 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-Methyl-benzyl)-5-(2-nitro-ethyl)-thiophene | HCID 59255460 | 43.4% |
Reaction Steps
To a dimethyl sulfoxide (20.0 mL) solution of 2-(4-methyl-benzyl)-5-((E)-2-nitro-vinyl)-thiophene (1.20 g, 4.63 mmol) described in Manufacturing Example 92-1-3 and acetic acid (1.20 mL) was added sodium borohydride (280 mg, 7.41 mmol) at room temperature while cooling appropriately under nitrogen atmosphere, which was stirred for 20 minutes at room temperature. Water was then added dropwise at room temperature while cooling appropriately. The reaction mixture was extracted with ethyl acetate, and the organic layer was washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was crystallized with a tetrahydrofuran-ethyl acetate-heptane system and filtered to obtain the title compound (525 mg, 43.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07691882B2 |
|---|
| Source dataset | uspto-grants-2010_04 |
|---|
| ORD ID | ord-b56754d7e1e645f4af239214a6082c11 |
|---|
| Source note | uspto-grants-2010_04 |
|---|