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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472786Generated: October 26, 2026

Dimethylformamide → Methyl 6-formyl-1-naphthoate

https://huagongshe.com/reaction/472786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
ReactantTrioctylsilane, 95%HCID 87780—
ReactantMethyl 6-(((trifluoromethyl)sulfonyl)oxy)-1-naphthoateHCID 22622428—
ReactantHCID 178418416HCID 178418416—
Catalystpalladium(II) acetateHCID 167845—
ProductMethyl 6-formyl-1-naphthoateHCID 5805697936%

Reaction Conditions

Temperature70 °C

Reaction Steps

Carbon monoxide (CO) gas was slowly bubbled through a solution of methyl 6-(((trifluoromethyl)sulfonyl)oxy)-1-naphthoate (334 mg, 1.0 mmol), Pd(OAc)2 (22 mg, 0.10 mmol), 1,3-bis-(diphenylphosphino)propane (40 mg, 0.10 mmol) and triethylamine (0.28 mL, 2.0 mmol) an DMF (8.3 mL). After 15 min, trioctylsilane (0.90 mL, 2.0 mmol) was added as bubbling continued. The mixture was heated at 70° C., continuing to bubble CO into the solution. After 6 h at 70 the bubbling CO was replaced with a balloon of CO and the reaction mixture was stirred overnight. After 18 h at 70° C., the reaction was cooled to room temperature, diluted with EtOAc (150 mL) and washed with water (3×50 mL) and brine (50 mL). The organic phase was dried (Na2SO4), filtered and concentrated in vacuo. The resulting residue was purified on 40 g silica gel (100% hexanes→25% EtOAc/hexanes, gradient) to afford 78 mg (36%) of methyl 6-formyl-1-naphthoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633220B2
Source datasetuspto-grants-2014_01
ORD IDord-f1f9697f468c45b4bb16255818f39e02
Source noteuspto-grants-2014_01