HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1190282Generated: October 31, 2026
Chloroacetaldehyde → HCID 58204096, compound
https://huagongshe.com/reaction/1190282
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178457530 | HCID 178457530 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58204096 | HCID 58204096 | 96.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08673952B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-81b2aba11c7341a292b373e342f36eae |
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| Source note | uspto-grants-2014_03 |
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