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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293470Generated: October 30, 2026

Sodium borohydride → HCID 10045440, compound

https://huagongshe.com/reaction/1293470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 10476669HCID 10476669—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10045440HCID 1004544066%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238725B2
Source datasetuspto-grants-2007_07
ORD IDord-43b1038c26ff45feabd295d0be3f33b1
Source noteuspto-grants-2007_07