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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872374Generated: October 26, 2026

Hydrochloric Acid → HCID 53951463, compound

https://huagongshe.com/reaction/1872374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant1-BromooctaneHCID 8140—
Reactant(3S)-2-((tert-butoxy)carbonyl)-7-hydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acidHCID 6712312—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
SolventSodium HydroxideHCID 14798—
ProductHCID 53951463HCID 53951463—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of (S)-2-Tert-butoxycarbonyl-1,2,3,4-tetrahydro-7-hydroxyisoquinoline-3-carboxylic acid (1 g) in a mixture of 10% NaOH aqueous solution (2.73 ml) and dimethylsulfoxide (11 ml) was stirred for half an hour at 80° C. Then, octyl bromide (0.589 ml) was added thereto, and stirred for 4 hours at 60° C. The reaction mixture was added to a mixture of water and ethyl acetate, and adjusted to pH 2.5 with conc. hydrochloric acid. The organic layer was taken, and dried over magnesium sulfate. The magnesium sulfate was filtered off, and the filtrate was evaporated under reduced pressure to give (S)-2-Tert-butoxycarbonyl-1,2,3,4-tetrahydro-7-octyloxyisoquinoline-3-carboxylic acid (1.30 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06107458
Source datasetuspto-grants-2000_08
ORD IDord-502ce3ce3e954d5c893605dca2155dc4
Source noteuspto-grants-2000_08