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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401696Generated: October 30, 2026

Benzaldehyde → HCID 59625807, compound

https://huagongshe.com/reaction/401696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium HydroxideHCID 14798—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1H-Indole-5-carboxylic acid, 2,3-dihydro-, methyl ester, hydrochloride (1:1)HCID 53408304—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 59625807HCID 5962580772.4%

Reaction Steps

A solution of methyl 2,3-dihydro-1H-indole-5-carboxylate HCl salt 55a (88.6 mg, 0.42 mmol), and benzaldehyde 23a (0.060 mL, 0.55 mmol) in CH2Cl2 (4 mL) was stirred at room temperature for 30 min. Sodium triacetoxyborohydride (159 mg, 0.75 mmol) was added to the mixture and stirring was continued for 2 h. Water was added to the resulting mixture at 0° C., and pH of the solution was adjusted to ˜8 with 1N aqueous NaOH. The mixture was extracted with CH2Cl2 and the organic layer was washed with brine and dried over Na2SO4. The solution was concentrated and purified by flash column chromatography (silica gel, 10-25% EtOAc/Heptanes) to give 55e (81.3 mg). MS m/z (M+H+) 268.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741887B2
Source datasetuspto-grants-2014_06
ORD IDord-2169a3d990bc4fe6875419cbc9f46be5
Source noteuspto-grants-2014_06