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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204186Generated: November 1, 2026

Silane, ((1-methoxy-2-methyl-1-propenyl)oxy)trimethyl- → Tert-butyl 3-methoxy-4-(1-methoxy-2-methyl-1-oxopropan-2-yl)benzoate

https://huagongshe.com/reaction/2204186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSilane, ((1-methoxy-2-methyl-1-propenyl)oxy)trimethyl-HCID 552336—
Reactanttert-Butyl 4-bromo-3-methoxybenzoateHCID 25307097—
CatalystZinc(II) fluorideHCID 10129912—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 3-methoxy-4-(1-methoxy-2-methyl-1-oxopropan-2-yl)benzoateHCID 58550749—

Reaction Steps

To a microwave vial was added ZnF2 (36 mg, 0.35 mmol) and Pd(tBu3P)2 (7.2 mg, 0.014 mmol). The reaction vessel was purged with nitrogen for 10 minutes before tert-butyl 4-bromo-3-methoxy-benzoate (200 mg, 0.70 mmol) dissolved in DMF (2.5 mL) was added followed by (1-methoxy-2-methyl-prop-1-enoxy)-trimethyl-silane (180 mg, 1.1 mmol). The reaction vessel was placed in an 80° C. oil bath under an atmosphere of nitrogen and the mixture was allowed to stir overnight. The mixture was allowed to cool to rt and was filtered through a frit and was washed with brine and EtOAc. The organics were separated and dried over sodium sulfate. The solvent was removed and the residue was taken on to the next step without additional purification. ESI-MS m/z calc. 308.2, found 309.4 (M+1)+; Retention time: 3.12 minutes (4 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365588B2
Source datasetuspto-grants-2016_06
ORD IDord-34dbda955b86410cb3f7ecff5208401e
Source noteuspto-grants-2016_06