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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436948Generated: October 30, 2026

Carbon Dioxide → 3-Methyl-2-buten-1-OL

https://huagongshe.com/reaction/436948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantFormaldehydeHCID 712—
ReactantIsobutyleneHCID 8255—
ReactantSodium SulfiteHCID 24437—
CatalystFormaldehydeHCID 712—
CatalystSodium Phosphate, DibasicHCID 24203—
SolventMethanolHCID 887—
Solventtert-ButanolHCID 6386—
Product3-Methyl-2-buten-1-OLHCID 11173—
Product3-Methyl-3-buten-1-olHCID 12988—

Reaction Conditions

Temperature200 °C

Reaction Steps

In a stainless steel autoclave having an inner volume of 300 ml, 9.0 g of paraformaldehyde of 95% purity, 0.22 g of sodium hydrogenphosphate as catalyst, and 60 ml of t-butanol were placed and the autoclave was closed. While cooling the autoclave with a dry ice and methanol mixture, the air in the autoclave was replaced by nitrogen and then 150 ml of isobutene was added thereto. Then the autoclave was brought to room temperature and no leak was found. Then the mixture was reacted with stirring at 200° C. for 4 hours. After the reaction, the autoclave was cooled and the contents were taken off. The reaction product was pale yellow and no substance having high boiling point was found. The reaction product was analyzed quantitatively by gas chromatography. Conversion of paraformaldehyde was determined by the sodium sulfite method. Conversion of paraformaldehyde was 98.9 mole%, and there were obtained 85.0 mole% of 3-methyl-3-butene-1-ol and 5.9 mole% of 3-methyl-2-butene-1-ol based on the paraform-aldehyde reacted. Total selectivities for the unsaturated alcohols were 90.9 mole% and no 4,4-dimethylmetadioxane was produced.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04028424
Source datasetuspto-grants-1977_06
ORD IDord-b0c4fc19f260490295aa3fadda1f4c8b
Source noteuspto-grants-1977_06