Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431185Generated: October 25, 2026

Sodium Hydroxide → CID 10898559

https://huagongshe.com/reaction/431185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
ReactantDtxcid5024346HCID 5311498—
ReactantTrimethylsulfoxonium BromideHCID 11126750—
CatalystFerrous sulfate heptahydrateHCID 62662—
SolventWaterHCID 962—
SolventMethyl Ethyl KetoneHCID 6569—
ProductCID 10898559HCID 10898559—

Reaction Conditions

Temperature35 °C

Reaction Steps

To 130 ml of ion-exchanged water were added 10 g of cyanocobalamin, 3.83 g of trimethylsulfoxonium bromide, 700 mg of iron (II) sulfate heptahydrate and 7.5 ml of 2-butanone. After replacing the atmosphere of the system by nitrogen, the mixture was heated in a water bath and a solution of sodium borohydride (4 g)/2N sodium hydroxide (0.2 ml)/water (20 ml) was added dropwise thereto under stirring at an inner temperature of 35° C. After stirring for 3 hours as it was, the mixture was cooled to 15° C. and then stirred overnight. Thereto was added 7.5 ml of 2-butanone, followed by stirring for 2 hours. Then, the precipitates were collected by filtration and dried, to give a crude product of the title compound. Thereto was added 140 ml of a 50% acetone aqueous solution, and the mixture was heated at 45° C., filtered and washed with 60 ml of a 50% acetone aqueous solution. After the mixture was adjusted to pH 6.5 with concentrated hydrochloric acid, 475 ml of acetone was added dropwise thereto and the mixture was stirred at 20° C. overnight. Precipitated crystals were collected by filtration and dried, to give 8.86 g of the title compound (yield 89.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06657057B2
Source datasetuspto-grants-2003_12
ORD IDord-8b588dda5088493bbea04d6df363b1fd
Source noteuspto-grants-2003_12