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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650996Generated: October 29, 2026

Thiophene → HCID 70360094, compound

https://huagongshe.com/reaction/1650996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
ReactantGlycine, N-methyl-, hydrochloride (1:1)HCID 69483—
Reactant2,3,4,4a,10,10a-Hexahydrophenanthren-9(1H)-oneHCID 290358—
ReactantPotassium FluorideHCID 522689—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 70360094HCID 7036009493.8%

Reaction Steps

A mixture of 46.4 parts of 2,3,4,4a,10,10a-hexahydro-9(1H)phenanthrenone, 58 parts of methyl glycine monohydrochloride, 2 parts of a solution of thiophene in methanol 4%, 480 parts of methanol and 26.1 parts of potassium fluoride was hydrogenated at normal pressure and at 50° C. with 3.0 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 1,1'-oxybisethane. The whole was treated with a sodium hydroxide solution. The separated organic layer was dried, filtered and evaporated, yielding 59.5 parts (93.8%) of methyl N-(1,2,3,4,4a,9,10,10a-octahydro-9-phenanthrenyl)glycine as a residue (int. 6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04927449
Source datasetuspto-grants-1990_05
ORD IDord-5c1baf4c19714ba790ec4ebc584c831a
Source noteuspto-grants-1990_05