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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296217Generated: October 25, 2026

Sodium Formate → Tert-butyl (5-formyl-2-methoxybenzyl)carbamate

https://huagongshe.com/reaction/1296217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium FormateHCID 2723810—
ReactantTert-butyl (5-bromo-2-methoxybenzyl)carbamateHCID 22926030—
CatalystTriphenylphosphineHCID 11776—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
SolventHCID 178418416HCID 178418416—
ProductTert-butyl (5-formyl-2-methoxybenzyl)carbamateHCID 2249393175.1%

Reaction Steps

1.015 g of t-butyl N-(5-bromo-2-methoxybenzyl)carbamate, 45 mg of dichlorobis(triphenylphosphine)palladium (II), 330 mg of sodium formate and 17 mg of triphenylphosphine were dissolved in anhydrous N,N-dimethylformamide, followed by stirring for 2 hours at 110° C. in carbon monoxide atmosphere. The reaction mixture was diluted with ethyl acetate, and washed with water and saturated sodium bicarbonate water. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated. The residue was purified by silica gel column chromatography, and 640 mg of t-butyl N-(5-formyl-2-methoxybenzyl)carbamate was obtained from fractions eluted with hexane-ethyl acetate (3:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244861B2
Source datasetuspto-grants-2007_07
ORD IDord-04a0c5bca7cd4ea2a1e72ff93846ae5a
Source noteuspto-grants-2007_07