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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587006Generated: October 30, 2026

Water → HCID 69747188, compound

https://huagongshe.com/reaction/587006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanto-FluorobenzaldehydeHCID 67970—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactantmethyl 7-[4-(2-butoxyethoxy)phenyl]-2,3-dihydro-1H-1-benzazepine-4-carboxylateHCID 22328987—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 69747188HCID 69747188100%

Reaction Steps

To a solution of methyl 7-(4-butoxyethoxyphenyl)-2,3-dihydro-1-benzazepine-4-carboxylate (300 mg) and 2-fluorobenzaldehyde (471 mg) in 1,2-dichloroethane (10 ml) was added sodium triacetoxyborohydride (402 mg), and the mixture was stirred under nitrogen atmosphere at room temperature for 5 days. Then, water was added to the mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried with magnesium sulfate. The solvent was evaporated under reduced pressure, and the resulting residue was purified with silica gel column chromatography (hexane:ethyl acetate=3:1) to give methyl-7-(4-butoxyethoxyphenyl)-1-(2-fluorobenzyl)-2,3-dihydro-1-benzazepine-4-carboxylate (382 mg) as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936602B1
Source datasetuspto-grants-2005_08
ORD IDord-d9b92828b7f84401b20dc570a9c1a873
Source noteuspto-grants-2005_08