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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383050Generated: October 29, 2026

Benzaldehyde → Ethyl 2-benzyl-1,2,3,4-tetrahydroisoquinoline-1-carboxylate

https://huagongshe.com/reaction/2383050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium HydroxideHCID 14798—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantEthyl 1,2,3,4-tetrahydroisoquinoline-1-carboxylate--hydrogen chloride (1/1)HCID 44890894—
SolventAcetic AcidHCID 176—
ProductEthyl 2-benzyl-1,2,3,4-tetrahydroisoquinoline-1-carboxylateHCID 5939619232.7%

Reaction Steps

In an ice bath, sodium triacetoxyborohydride (6.11 g) was added to a solution of ethyl 1,2,3,4-tetrahydroisoquinoline-1-carboxylate hydrochloride (4.98 g) and benzaldehyde (2.72 g) in acetic acid (50 mL). The mixture was stirred at room temperature for 15 hours. A 1 M aqueous NaOH solution was added to the reaction liquid which was then extracted with chloroform. The extract was washed with water and saturated brine, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane-EtOAc) to obtain ethyl 2-benzyl-1,2,3,4-tetrahydroisoquinoline-1-carboxylate (1.99 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263607B2
Source datasetuspto-grants-2012_09
ORD IDord-a3547cb828a04d2caed2484a33e1fc11
Source noteuspto-grants-2012_09