Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372409Generated: October 25, 2026

Methallyl alcohol → 2-Methyl-1,4-butanediol

https://huagongshe.com/reaction/372409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethallyl alcoholHCID 10557—
ReactantHCID 12270516HCID 12270516—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178505374HCID 178505374—
SolventWaterHCID 962—
Product2-Methyl-1,4-butanediolHCID 1805370%
Productbeta-Methyl-gamma-butyrolactoneHCID 984514%

Reaction Steps

The process is carried out as in Examples 1 - 5 using 50.0 grams of a methanolic co-distillate (boiling range 66° - 78° C) containing 14.8 grams of 2-methoxy-4-methyltetrahydrofuran derived from methallyl alcohol as described in step (a), 30 ml of water and 5.0 grams of powdered copper chromite (Catalysts and Chemicals Co.). The mixture is heated at 180° C under 1000 psi of hydrogen for one hour. Analysis of the product mixture shows the presence of 9.3 grams of 2-methyl-1,4-butandiol (70% yield) and about 0.5 grams of 3-methyl-4-butyrolactone (4% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04091041
Source datasetuspto-grants-1978_05
ORD IDord-b5220fa9d52240789ee45f8917821a5c
Source noteuspto-grants-1978_05