HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293470Generated: October 30, 2026
Sodium borohydride → HCID 10045440, compound
https://huagongshe.com/reaction/1293470
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 10476669 | HCID 10476669 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10045440 | HCID 10045440 | 66% |
Reaction Steps
N-Formyl-1-methoxy-4-[4-methoxyphenylaminosulphonyl]-9H-carbazole (example 70) (0.1 g, 0.24 mM) was dissolved in 18 mL of 20% aqueous THF solution. The reaction mixture was cooled to 0° C. in an ice bath. To it was added NaBH4 (0.055 g, 1.45 mM) portion wise. The reaction mixture was stirred overnight Solvent was evaporated and the aqueous layer was extracted with EtOAc. The organic layer was washed with brine and dried over anh. Na2SO4. It was filtered and concentrated to yield the crude product. The crude product was purified over a silica gel column using EtOAc- hexane as a solvent system to yield the desired compound as a white semi-solid with a yield of 66% (0.062 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07238725B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-43b1038c26ff45feabd295d0be3f33b1 |
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| Source note | uspto-grants-2007_07 |
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