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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383985Generated: October 30, 2026

Sodium borohydride → HCID 67369877, compound

https://huagongshe.com/reaction/383985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 67367547HCID 67367547—
SolventEthanolHCID 702—
ProductHCID 67369877HCID 67369877—

Reaction Steps

0.65 g (17.1 mmol) of NaBH4 were added in portions to a solution of 3.2 g (max. 14.2 mmol) of the crude product 7-fluoro-1-phenyl-3,4-dihydroisoquinoline in EtOH (80 ml) and the mixture was then stirred for 16 h at RT. Then the mixture was concentrated to small volume under vacuum and the residue was taken up with DCM (200 ml). It was washed with water and the aqueous phase was extracted with DCM (2×150 ml). The combined organic phases were washed with brine, dried over Na2SO4, filtered and concentrated to small volume under vacuum. 7-Fluoro-1-phenyl-1,2,3,4-tetrahydroisoquinoline was obtained as the crude product, which was reacted further with no additional purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367700B2
Source datasetuspto-grants-2013_02
ORD IDord-4138668e6cef4e1d9b10c6c7ce60c519
Source noteuspto-grants-2013_02