HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572258Generated: November 1, 2026
Sodium borohydride → HCID 58297378, compound
https://huagongshe.com/reaction/572258
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 58297374 | HCID 58297374 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58297378 | HCID 58297378 | 25% |
Reaction Steps
To an ice cooled solution of (E)-ethyl 3-(1-(4-bromophenyl)-2-(4-carbamoyl-2-methylphenyl)-1H-pyrrol-3-yl)acrylate (400 mg, 0.88 mmol) in 95% ethanol (10 mL) were added BiCl3 (554 mg, 1.76 mmol) and portionwise NaBH4 (134 mg, 3.52 mmol), then the resultant mixture was stirred at room temperature for 12 h. The reaction mixture was filtered, and the filtrate was partitioned between water (50 mL) and ethyl acetate (30 mL), the aqueous layer was extracted with ethyl acetate (30 mL×2). The combined organic layers were washed with brine, dried over sodium sulfate, and evaporated. The residue was purified by preparative TLC (eluting with 50% ethyl acetate in petroleum ether for three times) to give ethyl 3-(1-(4-bromophenyl)-2-(4-carbamoyl-2-methylphenyl)-1H-pyrrol-3-yl)propanoate (5-2) (100 mg, yield: 25%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029402B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-f68af790680e47a7804b78c959d83bf3 |
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| Source note | uspto-grants-2015_05 |
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