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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947283Generated: November 1, 2026

Hydrochloric Acid → Methyl 3-acetyl-4-hydroxybenzoate

https://huagongshe.com/reaction/1947283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantButyl vinyl etherHCID 8108—
ReactantTriethylamineHCID 8471—
ReactantMethyl 3-bromo-4-hydroxybenzoateHCID 4778958—
Catalystpalladium(II) acetateHCID 167845—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-acetyl-4-hydroxybenzoateHCID 1233283382%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a degassed solution of methyl 3-bromo-4-hydroxybenzoate (350 g, 1514.87 mmol) in ethanol (3 L) were added triethylamine (0.528 L, 3787.17 mmol), 1-(vinyloxy)butane (0.588 L, 4544.60 mmol), 1,1′-bis(diphenylphosphino)ferrocene (33.1 g, 60.6 mmol) and diacetoxypalladium (8.50 g, 37.9 mmol) under nitrogen. The mixture was heated at 70° C. overnight. The reaction was cooled down, filtered and the filtrate concentrated. The resulting solid was solubilized with DCM (2 L) and HCl 4N (1.14 L, 4544 mmol) was added under stirring. Stirring was maintained for 2 hrs, the organic phase was separated, dried over magnesium sulfate, filtered and concentrated to afford a solid which was stirred in diethyl ether (5 L) for 2 hrs. The solid was filtered off and the filtrate concentrated to dryness to afford methyl 3-acetyl-4-hydroxybenzoate (240 g, 82%) as a beige powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399460B2
Source datasetuspto-grants-2013_03
ORD IDord-b18586b0cd7b42e78f19002f0bd3c654
Source noteuspto-grants-2013_03