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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076009Generated: October 30, 2026

Strigol → HCID 616817, compound

https://huagongshe.com/reaction/1076009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStrigolHCID 5281396—
Reactant2,6,6-Trimethyl-3-oxocyclohex-1-ene-1-carboxylic acidHCID 15377700—
ReactantHCID 178501492HCID 178501492—
ProductHCID 616817HCID 616817—

Reaction Steps

A process for preparing dl-strigol, a potent seed germination agent, which comprises preparing the 2-bromomethyl-substituted methyl ester of 2,6,6-trimethylcyclohex-1-en-3-one-1-carboxylic acid, alkylating and cyclizing the said compound with an excess of dimethyl sodiomalonate to obtain methyl 1,4-diketo-7,7-dimethyl-4,5,6,7-tetrahydroindane-2-carboxylate and its enol, subjecting the said keto and enol forms of the compound, in admixture, to alkylation with methyl bromoacetate followed by acidic hydrolysis and spontaneous decarboxylation to obtain methyl 1,4-diketo-7,7-dimethyl-4,5,6,7-tetrahydroindane-2-acetic acid, reducing the said acetic acid with a hydride reducing agent and recovering and separating the resulting 1,4-cis and trans-dihydroxy-7,7-dimethyl-4,5,6,7-tetrahydroindane-2-acetic acid lactones, formylating each of the cis and trans γ lactones, alkylating the respective resulting hydroxy methylene lactones with bromobutenolide and recovering dl-strigol, dl-4'-epi-strigol, dl-4-epi-strigol and dl-4,4'-diepi-strigol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03954806
Source datasetuspto-grants-1976_05
ORD IDord-9f21579842834ddc9d825fc7110ce1e8
Source noteuspto-grants-1976_05