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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260566Generated: October 27, 2026

Water → 4-Acetoxy-2-methyl-2-buten-1-ol formate

https://huagongshe.com/reaction/260566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium FormateHCID 2723810—
Reactant4-Chloro-3-methylbut-2-en-1-yl acetateHCID 53400932—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDimethylformamideHCID 6228—
Product4-Acetoxy-2-methyl-2-buten-1-ol formateHCID 5433524495%

Reaction Conditions

Temperature40 °C

Reaction Steps

4-Acetoxy-2-methyl-1-chloro-2-butene (8.13 g, 50 mmol) was dissolved in dimethylformamide (25 ml) and placed in a 100 ml four neck flask. To this were added sodium formate powder (6.80 g, 100 mmol, 2 equivalents) and tetra n-butylammonium bromide (0.81 g, 2.5 mmol, 5 mol %). The mixture was stirred at 40° C. for 24 hours under heating. After completion of the reaction, the reaction mixture was poured into ice-cooled water (about 30 ml) and extracted with ether (50 ml) three times. The extracted ether layer was dried over anhydrous sodium sulfate. Evaporation of the ether followed by purification by silica gel column chromatography (ethyl acetate-hexane (=1:3)) gave 4-acetoxy-2-methyl-2-buten-1-ol formate (8.18 g, 47.5 mmol; Yield: 95.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05527952
Source datasetuspto-grants-1996_06
ORD IDord-8d2be91cd4814da2b50f692d6d4747a7
Source noteuspto-grants-1996_06