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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340880Generated: October 31, 2026

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

https://huagongshe.com/reaction/340880

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 numberUS08895582B2
Source datasetuspto-grants-2014_11
ORD IDord-cc82baa8535e4af0abd1b5c6d16303c5
Source noteuspto-grants-2014_11