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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019492Generated: October 26, 2026

1,3-Butadiene → HCID 86661434, compound

https://huagongshe.com/reaction/1019492

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-ButadieneHCID 7845—
Reactant3-Buten-1-olHCID 69389—
Reactantacetyl CoAHCID 444493—
ReactantMalonyl CoAHCID 644066—
ReactantPenta-2,4-dienoateHCID 73155734—
ProductHCID 86661434HCID 86661434—

Reaction Steps

Pathways to 3-butene-1-ol, butadiene and 2,4-pentadienoate from malonyl-CoA and acetyl-CoA are shown in FIG. 21. In these pathways, malonyl-CoA and acetyl-CoA are joined by a thiolase to form 3-oxoglutaryl-CoA. This intermediate can then be converted to 3,5-dihydroxypentanoate by several alternate routes (Steps B/C/D, Steps B/G, Steps H/I/J, Steps H/L/D, K/J). Once formed, 3,5-dihydroxypentanoate can be decarboxylated by a 3-hydroxyacid decarboxylase to form 3-butene-1-ol (Step M). Subsequent dehydration by a 3-butene-1-ol dehydrogenase or a chemical catalyst yields butadiene (Step O). Alternately, 3,5-dihydroxypentanoate can be dehydrated to 5-hydroxypent-2-enoate as shown in Step E. This intermediate can then be decarboxylated to 3-butene-1-ol (Step N) or further dehydrated to 2,4-pentadienoate (Step F).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08715957B2
Source datasetuspto-grants-2014_05
ORD IDord-6c55b5697992423b96a698721edb17eb
Source noteuspto-grants-2014_05