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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100637Generated: October 30, 2026

Benzaldehyde → (+/-)-trans-2-Benzyl-6-(trifluoromethyl)-2,3,3a,4-tetrahydro-1H-pyrrolo[3,4-c]isoquinolin-5(9bH)-one

https://huagongshe.com/reaction/2100637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(+/-)-trans-6-(trifluoromethyl)-2,3,3a,4-tetrahydro-1H-pyrrolo[3,4-c]isoquinolin-5(9bH)-oneHCID 57799321—
ReactantHCID 86090086HCID 86090086—
CatalystAcetic AcidHCID 176—
Solvent1,2-DichloroethaneHCID 11—
SolventSodium BicarbonateHCID 516892—
Product(+/-)-trans-2-Benzyl-6-(trifluoromethyl)-2,3,3a,4-tetrahydro-1H-pyrrolo[3,4-c]isoquinolin-5(9bH)-oneHCID 6905211783%

Reaction Steps

To a solution of (±)-trans-6-(trifluoromethyl)-2,3,3a,4-tetrahydro-1H-pyrrolo[3,4-c]isoquinolin-5(9bH)-one, the free base of Example 10, (161 mg, 0.63 mmol) in 4 mL of 1,2-dichloroethane was added benzaldehyde (0.076 mL, 0.76 mmol), sodium triacetoxyborohydride (267 mg, 1.26 mmol) and 3 drops of glacial acetic acid. The mixture was allowed to stir at ambient temperature for 3 h. The reaction was diluted with sat'd aq NaHCO3 and extracted with ethyl acetate. The organics were washed with brine, dried (MgSO4) and concentrated in vacuo to afford 180 mg (83%) of the title compound which was sufficiently pure to be used without purification. LRMS (ESI): 347.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572805B2
Source datasetuspto-grants-2009_08
ORD IDord-cfe58908f26341408f1fff073f2291b6
Source noteuspto-grants-2009_08