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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416359Generated: November 2, 2026

Hydrochloric Acid → HCID 15314191, compound

https://huagongshe.com/reaction/1416359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,1-Dimethylethyl 5-ethoxy-3,4-dihydro-2(1H)-isoquinolinecarboxylateHCID 15434299—
SolventEthanolHCID 702—
ProductHCID 15314191HCID 15314191—

Reaction Steps

Excess of 3 mol L-1 hydrochloric acid in ethanol was added to a solution of 2-t-butoxycarbonyl-5-ethoxy-1,2,3,4-tetrahydroisoquinoline (Example 8) (1.55 g, 5.6 mmol) in ethanol. After 3 hours, the solution was evaporated to dryness, and the hydrochloride salt of 5-ethoxy-1,2,3,4-tetrahydroisoquinoline was dissolved in water. The solution was made strongly alkaline with sodium hydroxide, and the product was extracted in dichloromethane, dried over Na2SO4, and evaporated. The product was purified by recrystallization from absolute ethanol. Yield 0.69 g, 71%. 1H NMR (DMSO-d6, 500 MHz): 7.02 (1H, t, 7.8 Hz). 6.70 (1H, d, 8.0 Hz), 6.57 (1H, d, 7.2 Hz), 3.98 (2H, q, 6.9 Hz), 3.77 (2H, s), 3.24 (2H, s), 2.91 (2H, s), 1.31 (3H, t, 6.9 Hz); 13C NMR (DMSO-d6, 120 MHz): 156.1, 137.5, 125.7, 123.5, 118.1, 108.2, 62.9, 47.7, 43.0, 23.1, 14.7; MS(EI+): 177 (95%, M+), 148 (100%), 132 (25%), 120 (43%), 104 (56%), 91 (33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05912342
Source datasetuspto-grants-1999_06
ORD IDord-71eb29ad43d24408a67aaef80eee7b77
Source noteuspto-grants-1999_06