HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078221Generated: October 29, 2026
3,3,3-Triethoxyprop-1-yne → 1-Bromo-4-chloro-2-(3,3,3-triethoxyprop-1-ynyl)benzene
https://huagongshe.com/reaction/2078221
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,3,3-Triethoxyprop-1-yne | HCID 10920972 | — |
| Reactant | 1-Bromo-4-chloro-2-iodobenzene | HCID 51000072 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Bromo-4-chloro-2-(3,3,3-triethoxyprop-1-ynyl)benzene | HCID 67099920 | 91% |
Reaction Steps
A suspension of 1-bromo-4-chloro-2-iodobenzene (2.5 g, 7.9 mmol), 3,3,3-triethoxyprop-1-yne (2.4 g, 13.9 mmol), copper(I) iodide, (455 mg, 2.3 mmol), and trans-dichlorobis(triphenylphosphine)palladium(II) (559 mg, 0.79 mmol) was treated with ACN (30 mL). The reaction was capped, evacuated under vacuum, backfilled with argon, and treated with TEA (9.9 mL, 71.6 mmol). The reaction was stirred at 23° C. After 2 hours, the reaction mixture was concentrated in vacuo to remove all solvents, diluted with EtOAc (250 mL) and washed with brine (150 mL), dried over MgSO4, concentrated in vacuo and purified by silica gel chromatography (eluant: 4% EtOAc/hexane+1% TEA), affording 2.6 g of 1-bromo-4-chloro-2-(3,3,3-triethoxyprop-1-ynyl)benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07928139B2 |
|---|
| Source dataset | uspto-grants-2011_04 |
|---|
| ORD ID | ord-a57fd86e12f34a3b8f67afb55707cfcd |
|---|
| Source note | uspto-grants-2011_04 |
|---|