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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532870Generated: October 27, 2026

Diethyl Carbonate → HCID 86711379, compound

https://huagongshe.com/reaction/532870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl CarbonateHCID 7766—
ReactantLithium diisopropylamideHCID 2724682—
Reactant5-Iodo-1-methyl-3,4-dihydroisoquinolineHCID 86711315—
Reactant(Z)-ethyl 2-(5-iodo-3,4-dihydroisoquinolin-1(2H)-ylidene)acetateHCID 86711320—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86711379HCID 86711379—

Reaction Conditions

Temperature-78 °C

Reaction Steps

(Z)-ethyl 2-(5-iodo-3,4-dihydroisoquinolin-1(2H)-ylidene)acetate. To a yellow cooled solution of 5-iodo-1-methyl-3,4-dihydroisoquinoline (30.1 g, 111 mmol) in dry THF (900 mL) was added dropwise a solution of LDA (2M in THF, 111 mL, 222 mmol) at −78° C. The resulting brown solution was stirred for at −78° C. for 45 min and a solution of diethyl carbonate (14 mL, 116 mmol) in THF (80 mL) was then added dropwise. The mixture was stirred at −78° C. for another 45 min, and then poured onto brine. The resulting yellow suspension was filtered and the filter cake was washed with AcOEt. The filtrate was extracted with AcOEt, and the combined org. phases were dried over Na2SO4, filtered and concentrated in vacuo to give the title compound (40.0 g) as a brown oil that was used as it is in the next step. UPLC-MS: MS 344.1 (M+H+); UPLC rt 1.28 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853203B2
Source datasetuspto-grants-2014_10
ORD IDord-db39c10246384736b06b03f1c1c28c95
Source noteuspto-grants-2014_10