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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726434Generated: November 1, 2026

Phosphorus oxide (P4O10) → 1-Chloromethyl-6-methoxy-3,4-dihydro-isoquinolinium chloride

https://huagongshe.com/reaction/1726434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxide (P4O10)HCID 14812—
ReactantAcetamide, 2-chloro-N-(m-methoxyphenethyl)-HCID 214755—
SolventDiethyl EtherHCID 3283—
Product1-Chloromethyl-6-methoxy-3,4-dihydro-isoquinolinium chlorideHCID 66657077—

Reaction Steps

Two equiv. of P2O5 (12.9 g) was boiled in xylenes (180 mL) as a 0.25 M solution. The crude product from Step 1 above was also first boiled in xylenes (45 mL) to make a 0.5 M solution, and it was then added dropwise via an addition funnel to the P2O5 solution. The mixture was stirred and heated at reflux for 1 h. The reaction was then cooled to RT and the xylenes decanted off at this point. The flask was then placed in an ice bath and stirred while ice, water, EtOAc, and finally 4 M NaOH were added carefully until the pH>12. Reaction was kept <25° C. until pH=12 was reached. The reaction was then extracted with EtOAc (3×). The combined organic extracts were dried over MgSO4 and concentrated to give a dark solution. This was cooled in an ice bath while 400 mL of cold Et2O was added followed by 100 mL of cold HC1/Et2O. A precipitate formed and was filtered away, washing with Et2O. The solid was immediately placed on high vac for 2 h to give the target product as a colored foamy solid. This crude product was directly used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491794B2
Source datasetuspto-grants-2009_02
ORD IDord-36a31562957c499fa3c16088768acd61
Source noteuspto-grants-2009_02