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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383993Generated: November 1, 2026

Ammonium Chloride → 4,4-Dimethyl-1-phenyl-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/383993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
Reactant4,4-Dimethyl-1-phenyl-3,4-dihydroisoquinolineHCID 13728598—
SolventMethanolHCID 887—
Product4,4-Dimethyl-1-phenyl-1,2,3,4-tetrahydroisoquinolineHCID 566869784%

Reaction Steps

A solution of 471 mg (2.0 mmol) of 4,4-dimethyl-1-phenyl-3,4-dihydroisoquinoline in MeOH (6 ml) was cooled to 0° C. and 151 mg (4.0 mmol) of NaBH4 were added in portions. After stirring for 3 h at RT a saturated aqueous NH4Cl solution was added. Then most of the methanol was removed under vacuum and the residue was extracted with EE. The organic phase was washed with brine, dried over Na2SO4, filtered and concentrated to small volume under vacuum. 19 mg (0.08 mmol, 4%) of 4,4-dimethyl-1-phenyl-1,2,3,4-tetrahydroisoquinoline were obtained as the residue, 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-72e706a3014a4eb3aa429a5b55574ef3
Source noteuspto-grants-2013_02