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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238358Generated: October 30, 2026

Dichloromethane → HCID 68683499, compound

https://huagongshe.com/reaction/2238358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 68685035HCID 68685035—
ProductHCID 68683499HCID 68683499—

Reaction Steps

1-(4-bromo-benzyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline hydrochloride (33) was prepared as follows: 1-(4-bromo-benzyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline oxalate (1.24 g, 2.74 mmol) was added to a mixture of 50 mL CH2Cl2 and 50 ml of 1N NaOH. The reaction mixture was stirred at room temperature. After dissolving of precipitate, the organic phase was separated, dried over Na2SO4, filtered, and evaporated. A residue was dissolved in MeOH and 10 mL of 1M solution of HCl in Et2O was added. Hydrochloride was crystallized from MeOH-Et2O mixture. Yield is 0.958 g (87.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718672B2
Source datasetuspto-grants-2010_05
ORD IDord-9615244c90b04a3285ec1049923bb69a
Source noteuspto-grants-2010_05