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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397051Generated: October 30, 2026

Sodium borohydride → 6-Methoxy-1-thiophen-2-yl-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/397051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant6-Methoxy-1-thiophen-2-yl-3,4-dihydroisoquinolineHCID 10800286—
SolventMethanolHCID 887—
Product6-Methoxy-1-thiophen-2-yl-1,2,3,4-tetrahydroisoquinolineHCID 516323289%

Reaction Steps

Sodium borohydride (0.916 g, 24.2 mmol) was added in small portions to a solution of 6-methoxy-1-thiophen-2-yl-3,4-dihydroisoquinoline (1.470 g, 6.04 mmol) in MeOH (50 ml) at 0° C. The reaction mixture was stirred for 30 min, warmed to rt and stirred at rt for 21 hr, then quenched by the dropwise addition of H2O (10 ml). Excess MeOH was removed by evaporation and the resulting aqueous solution was extracted with CHCl3 (4×10 ml). The combined extracts were dried over MgSO4 and concentrated in vacuo to give 1.316 g (89% yield) of yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608203B2
Source datasetuspto-grants-2003_08
ORD IDord-512fec893adc4ee89ba59f9e1add20a5
Source noteuspto-grants-2003_08