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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926237Generated: October 26, 2026

Hydrochloric Acid → 5-Iodo-1-methyl-3,4-dihydroisoquinoline

https://huagongshe.com/reaction/926237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantOxalyl chlorideHCID 65578—
ReactantN-(2-iodophenethyl)acetamideHCID 86711313—
Reactant7-iodo-10b-methyl-5,6-dihydro-2H-oxazolo[2,3-a]isoquinoline-2,3(10bH)-dioneHCID 86711314—
SolventDichloromethaneHCID 6344—
Product5-Iodo-1-methyl-3,4-dihydroisoquinolineHCID 86711315—

Reaction Steps

7-iodo-10b-methyl-5,6-dihydro-2H-oxazolo[2,3-a]isoquinoline-2,3(10bH)-dione. A solution of N-(2-iodophenethyl)acetamide (16.0 g, 55.3 mmol) in DCM (600 mL) under N2, was treated dropwise with (COCl)2 (5.33 mL, 60.9 mmol). The reaction was stirred at RT for 45 min and then cooled to 0° C. FeCl3 (10.8 g, 66.4 mmol) was then added and the mixture was allowed to slowly warm to RT and stirred at RT for 18 h. An aq. solution of 2N HCl (50 mL) was added and the mixture was stirred for 2 h. The organic phase was separated, dried over Na2SO4, filtered and concentrated in vacuo to provide the title compound as a brown solid (20.8 g) that was used as it is in the next step. UPLC-MS: MS 344.3 (M+H+); UPLC rt 1.10 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284331B2
Source datasetuspto-grants-2016_03
ORD IDord-cd0d470aff3743f79c2a5c85023b8569
Source noteuspto-grants-2016_03