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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621388Generated: November 2, 2026

Hydrochloric Acid → HCID 178498868, compound

https://huagongshe.com/reaction/621388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl formateHCID 7865—
ReactantSodium hydrideHCID 24758—
ReactantPotassium thiocyanateHCID 516872—
Reactantmethyl N-(decahydro-1-naphthalenyl)-N-formylglycineHCID 86742951—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178498868HCID 178498868—

Reaction Steps

To a stirred solution of methyl N-(decahydro-1-naphthalenyl)-N-formylglycine in 900 parts of tetrahydrofuran and 127 parts of methyl formate were added suitable amounts of sodium hydride. After stirring for 18 hours at room temperature, 350 parts of deionisized water and 1.4 parts of 1,1'-oxybisethane were added to the mixture. The separated aqueous layer was acidified with 132.7 parts of concentrated hydrochloric acid and 280 parts of methanol were added. The whole was heated to 40°-50° C. and treated with a solution of 92.7 parts of potassium thiocyanate in 200 parts of deionisized water. The whole was stirred for 22 hours at room temperature. The precipitated product was filtered off and crystallized from methanol. The product was filtered off and dried, yielding methyl 2-mercapto-N-(decahydro-1-naphthalenyl)-1H-imidazole-5-carboxylate; mp. 179°-181° C. (compound 1.15).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04824472
Source datasetuspto-grants-1989_04
ORD IDord-80785f56f320434fb5b0c1e003a5c17d
Source noteuspto-grants-1989_04