Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587758Generated: November 2, 2026

Bicarbonate Ion → HCID 86746969, compound

https://huagongshe.com/reaction/1587758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBicarbonate IonHCID 769—
ReactantTriethylamineHCID 8471—
ReactantTert-Butyl hypochloriteHCID 521297—
ReactantHCID 86746962HCID 86746962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 86746969HCID 86746969—

Reaction Conditions

Temperature-40 °C

Reaction Steps

7.89 g of 6-cyano-2-morpholinomethyl-8beta-ergoline-carboxylic acid methyl ester (20 mmol) is dissolved in 400 ml of anhydrous tetrahydrofuran, the solution is cooled to -40° C., mixed with 4 ml of triethylamine and then the solution of 3.0 ml of tert-butyl hypochloride (25 mmol) in 60 ml of anhydrous tetrahydrofuran is instilled. After 10 minutes of stirring, another 1 ml of tert-butylhypochlorite is added, stirred for 5 minutes and the solution is poured on ice. The mixture is made alkaline with bicarbonate solution and shaken with ethyl acetate. The organic phases are dried, the solvent is evaporated and the residue is crystallized from the diisopropylether, the yield is quantitative [α]D =+42.7° (0.5% in chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05219862
Source datasetuspto-grants-1993_06
ORD IDord-5d153003905b490cb1d28c08267739d8
Source noteuspto-grants-1993_06