HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981828Generated: October 30, 2026
Dimethylformamide → HCID 20071127, compound
https://huagongshe.com/reaction/981828
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 5-Bromo-2-chloroanisole | HCID 2769567 | — |
| Reactant | Silane, [(3,4-dihydro-2-naphthalenyl)oxy]trimethyl- | HCID 11042217 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 20071127 | HCID 20071127 | — |
Reaction Steps
Charge an oven dried, argon flushed 25-mL 2-necked round bottomed flask equipped with a stirring bar and reflux condenser with 2-trimethylsilyloxy-3,4-dihydronaphthalene (0.4247 grams, 1.9449 mmoles) and tetra-n-butylammonium fluoride (2.3 mL, 2.30 mmoles, 1 M in tetrahydrofuran), stir for a few minutes and then add 4-bromo-2-methoxy-1-chlorobenzene (0.4336 grams, 1.9577 mmoles) dichlorobis(tri-ο-tolyl-phosphine)palladium (0.0154 grams, 0.0196 mmoles) and 5 mL dimethylformamide. Heat the reaction mixture for 18 hours (oil bath temperature about 90° C.), cool to RT and add 5 mL water and 10 mL t-butylmethyl ether. Separate the layers, extract the aqueous layers with 3×5 mL t-butylmethyl ether, wash the combined organic layers with water and saturated salt solution, dry over magnesium sulfate and concentrate using a Buchi rotavapor to yield the final product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04992591 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-efd9e7c9dc0741e8a9157ed9e13ac00a |
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| Source note | uspto-grants-1991_02 |
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