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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409742Generated: October 30, 2026

Methanol → Methyl 6-fluoro-1,2,3,4-tetrahydroisoquinoline-3-carboxylate

https://huagongshe.com/reaction/409742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant6-Fluoro-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acidHCID 57947941—
ProductMethyl 6-fluoro-1,2,3,4-tetrahydroisoquinoline-3-carboxylateHCID 57947410—

Reaction Steps

To a suspension of 6-fluoro-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid in methanol (500 mL) was added SOCl2 (50 mL). The reaction mixture was then refluxed for 1 h until LC-MS indicated the completion of the reaction. The mixture was concentrated, and the resulting residue was dissolved in a mixture of EtOAc (1 L) and sat. sodium bicarbonate solution (500 mL). The organic layer was separated, washed with water and brine, dried over Na2SO4, and concentrated under reduced pressure to give 6-fluoro-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid methyl ester as an oil (92 g). LRMS (M+H+) m/z 210.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759374B2
Source datasetuspto-grants-2014_06
ORD IDord-472e69e60d9545f7b1af2a7a845815b2
Source noteuspto-grants-2014_06