HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773972Generated: November 1, 2026
4-Bromo-2-chloro-1-cyclopropoxybenzene → Tert-butyl 2-(3-chloro-4-cyclopropoxyphenyl)acetate
https://huagongshe.com/reaction/1773972
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromo-2-chloro-1-cyclopropoxybenzene | HCID 57594658 | — |
| Reactant | HCID 178451183 | HCID 178451183 | — |
| Catalyst | HCID 178418851 | HCID 178418851 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Tert-butyl 2-(3-chloro-4-cyclopropoxyphenyl)acetate | HCID 89649373 | — |
Reaction Steps
To a solution of 4-bromo-2-chloro-1-cyclopropoxy-benzene (610 mg, 2.46 mmol, 1.00 eq.) in dioxane (20 mL), bis(tri-t-butylphosphine)palladium (0) (193 mg, 0.37 mmol, 0.15 eq.) and 2-tert-butoxy-2-oxoethylzinc chloride (0.5M in diethyl ether) (8.9 mL, 4.44 mmol, 1.80 eq.) were added in sequence. The resulting mixture was stirred at r.t. for 18 hours and further at 60° C. for 4 hours. The mixture was allowed to cool down to r.t. and filtered through Celite. The filtrate was concentrated in vacuo. The residue was purified by flashmaster (column: 100 g, flow: 45 mL/min, 40 fractions of 45 mL, Heptane to Heptane+5% AcOEt) to yield the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09255090B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-f19b22be283240fe8b52cd77b05a1b92 |
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| Source note | uspto-grants-2016_02 |
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