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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587070Generated: October 30, 2026

Sodium triacetoxyborohydride → HCID 178450548, compound

https://huagongshe.com/reaction/587070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactantmethyl 7-[4-(2-butoxyethoxy)phenyl]-2,3-dihydro-1H-1-benzazepine-4-carboxylateHCID 22328987—
ReactantHCID 178520064HCID 178520064—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
ProductHCID 178450548HCID 17845054879.3%

Reaction Conditions

Temperature40 °C

Reaction Steps

In 1,2-dichloroethane (14 ml)/acetic acid (7 ml) was dissolved methyl 7-[4-(2-butoxyethoxy)phenyl]-2,3-dihydro-1-benzazepine-4-carboxylate (0.70 g). To the solution were added tetrazole-5-carbaldehyde (0.31 g) and sodium triacetoxyborohydride (1.5 g), and the mixture was stirred at 40° C. for 18 hours. The mixture was cooled to room temperature, and the solvent was removed under reduced pressure. The resulting residue was added to water, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried with magnesium sulfate. The solvent was removed under reduced pressure, and the resulting residue was purified with silica gel column chromatography (ethyl acetate/ethanol=15:1) to give methyl 7-[4-(2-butoxyethoxy)phenyl]-1-(tetrazol-5-ylmethyl)-2,3-dihydro-1-benzazepine-4-carboxylate (0.67 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936602B1
Source datasetuspto-grants-2005_08
ORD IDord-47f8e383ff964daabf9dccb92bbf3529
Source noteuspto-grants-2005_08