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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761663Generated: October 29, 2026

Hydrochloric Acid → HCID 178515745, compound

https://huagongshe.com/reaction/1761663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant2-Cyano-6-hydroxybenzothiazoleHCID 9881912—
ReactantD-Cysteine hydrochloride monohydrateHCID 10176341—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 178515745HCID 17851574589.3%

Reaction Steps

685 mg. (3.9 mMol) D-cysteine hydrochloride monohydrate are dissolved in 13 ml. water which has been previously gassed with nitrogen. A pH value of 8 is adjusted, under an atmosphere of nitrogen, with about 6 ml. of a 1N aqueous sodium hydroxide solution and then a solution of 528 mg. (3 mMol) 2-cyano-6-hydroxybenzothiazole in 22 ml. methanol (analytically pure) is added thereto under an atmosphere of nitrogen. The yellow solution is stirred under an atmosphere of nitrogen and with the exclusion of light for 1 hour at ambient temperature. Subsequently, the solution is acidified with 3 ml. of 2N hydrochloric acid and left to stand for about 3 hours at 4° C. The precipitated crystals are filtered off with suction under an atmosphere of nitrogen, washed with methanol and water (1:1 v/v) and dried in a desiccator with the exclusion of light. 0.75 g. D-Luciferin are obtained, which corresponds to a yield of 89.3% of theory. The compound melts at 187°-188° C., with decomposition, and is chromatographically identical with the product known from the literature but contains small amounts of impurities.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04826989
Source datasetuspto-grants-1989_05
ORD IDord-ebeaea12d238413dba497c4ea6e10a24
Source noteuspto-grants-1989_05