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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178413Generated: October 28, 2026

Sodium Cyanide → HCID 18431538, compound

https://huagongshe.com/reaction/1178413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 18425715HCID 18425715—
ReactantHCID 18425743HCID 18425743—
Catalyst15-Crown-5HCID 36336—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 18431538HCID 18431538—

Reaction Conditions

Temperature0 °C

Reaction Steps

24.9 (69.2 mmol) 4-(1-diphenylmethyl-piperidin-4-yl)-butan-1-ol hydrochloride are suspended in 160 ml absolute dichloromethane and cooled to ca. 0° C. under moisture exclusion. At this temperature, 16.0 g (159 mmol) TEA are first added and thereafter a solution of 0.3 g (90.0 mmol) methanesulfonoic acid chloride in a little absolute dichloromethane is added dropwise. The mixture is then subsequently stirred for three hours at RT and then placed in ice water. The organic phase is washed once with 50 ml water, dried over sodium sulfate and the solvent is removed under vacuum. The resulting methanesulfonoic acid-4-(1-diphenylmethyl-piperidin-4-yl)-butyl ester is dissolved in 120 ml DMF without further purification and with 7.7 g (158 mmol) sodium cyanide and two drops 15-crown-5 and stirred for six hours at 65° C. After cooling, the mixture is poured in ice water. The precipitated solid is drawn off and dried at 40° C. in high-vacuum. The solid is processed further without additional purification. Yield: 19.9 g (86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276524B2
Source datasetuspto-grants-2007_10
ORD IDord-06f74dd0313245f88b987c6d710a485a
Source noteuspto-grants-2007_10