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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1190282Generated: October 31, 2026

Chloroacetaldehyde → HCID 58204096, compound

https://huagongshe.com/reaction/1190282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178457530HCID 178457530—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58204096HCID 5820409696.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 8-bromo-N-isopropyl-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxamidine (878 mg, 2.4 mmol) in THF (15 mL) was added chloroacetaldehyde solution (˜50 wt. % in H2O, 7.53 mL, 47.9 mmol) and aqueous saturated sodium bicarbonate solution (6 mL) at RT. The mixture was heated to 80° C. with rapid stirring. After heating for 20 hours the mixture was allowed to cool to RT and was extracted with DCM (150 mL). The organic layer was washed with water followed by brine, dried (Na2SO4) and concentrated in vacuo. The resultant residue was purified by flash chromatography (SiO2, gradient 0-100% EtOAc in cyclohexane) to afford the title compound (900 mg, 96%). LCMS RT=4.90 min, [M+H]+=390/392

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673952B2
Source datasetuspto-grants-2014_03
ORD IDord-81b2aba11c7341a292b373e342f36eae
Source noteuspto-grants-2014_03