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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397038Generated: October 30, 2026

Sodium borohydride → HCID 18172410, compound

https://huagongshe.com/reaction/397038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 18172446HCID 18172446—
SolventMethanolHCID 887—
ProductHCID 18172410HCID 1817241099.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium borohydride (0.34 g, 0.89 mmol) was added in small portions to a solution of 1-(4-benzyloxyphenyl)-3,4-dihydroisoquinoline (0.139 g, 0.44 mmol) in MeOH (10 ml) at 0° C. The reaction mixture was stirred at 0° C. for 30 min, stirred at rt for 1 hr, then quenched by the dropwise addition of H2O (1.0 ml). The resulting mixture was concentrated in vacuo to remove the methanol, and the remaining aqueous layer was extracted with CHCl3 (4×10 ml). The combined extracts were dried over MgSO4 and concentrated in vacuo to give 0.138 g (99% yield) of colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608203B2
Source datasetuspto-grants-2003_08
ORD IDord-74bfd9601ac04e8c89d128cfd1fcc695
Source noteuspto-grants-2003_08