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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762042Generated: November 1, 2026

Thiophene → HCID 70360090, compound

https://huagongshe.com/reaction/1762042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
ReactantGlycine, N-methyl-, hydrochloride (1:1)HCID 69483—
ReactantCyclopent[a]inden-8(1H)-one, 2,3,3a,8a-tetrahydro-HCID 316916—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 70360090HCID 7036009086.9%

Reaction Steps

A mixture of 23.4 parts of 2,3,3a,8a-tetrahydrocyclopent[a]inden8(1H)-one, 31.4 parts of methyl glycine hydrochloride, 1 part of a solution of thiophene in methanol 4%, 400 parts of methanol and 13.3 parts of potassium acetate was hydrogenated at normal pressure and at room temperature with 2.0 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The residue was taken up in water and the product was extracted with dichloromethane. The extract was washed with a hydrochloric acid solution and a sodium hydroxide solution, dried, filtered and evaporated, yielding 29.0 parts (86.9%) of methyl N-(1,2,3,3a,8,8a-hexahydrocyclopent[a]inden-8-yl)-glycine as a residue (int. 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04830664
Source datasetuspto-grants-1989_05
ORD IDord-a73ef35d8ab7412fb5316d228f2ed943
Source noteuspto-grants-1989_05