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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436039Generated: October 29, 2026

Tetrahydrofuran → HCID 76851486, compound

https://huagongshe.com/reaction/1436039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 21979982HCID 21979982—
CatalystHCID 178527703HCID 178527703—
SolventEthanolHCID 702—
ProductHCID 76851486HCID 76851486102.1%

Reaction Steps

A solution of 4-bromo-1-chloro-5-nitroisoquinoline (14.0 g) prepared according to the method described in a known literature (Nair et al., Indian J. Chem., 1967, 5, 403) in ethanol (75 ml) and tetrahydrofuran (75 ml) was added with 3% platinum-sulfur/activated carbon (3% Pt-S/C, NE Chemcat, CM011, 14.0 g), and the mixture was stirred at room temperature for 15 hours under a hydrogen gas atmosphere. The atmosphere was replaced with nitrogen gas, and then the insoluble matters were removed by filtration through Celite, and the solvent was evaporated under reduced pressure to obtain the title compound (12.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618984B2
Source datasetuspto-grants-2009_11
ORD IDord-4df93a08615e47faaef2588eeb250695
Source noteuspto-grants-2009_11