Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860448Generated: October 31, 2026

Ethanol → HCID 10738521, compound

https://huagongshe.com/reaction/1860448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTriethylamineHCID 8471—
ReactantPivaloyl chlorideHCID 62493—
ReactantHCID 10085886HCID 10085886—
SolventDichloromethaneHCID 6344—
ProductHCID 10738521HCID 1073852149.1%

Reaction Steps

3.36 g (13.1 mmol) of 1,4-dibenzyl-2-aminomethylpiperazine prepared according to a protocol identical to the one used in steps 6.1 and 6.2 of Example 6 are dissolved in 5.5 ml (3 equivalents; 39.3 mmol) of triethylamine and 100 ml of dichloromethane and are treated by rapid dropwise addition of 2.63 ml (1.5 equivalents; 19.6 mmol) of 2,2-dimethylpropanoyl chloride dissolved in 30 ml of CH2Cl2. The solution is refluxed for 4 hours. A few ml of ethanol are then added, after which the solution is washed twice with water, once with saturated NaHCO3 solution and then with water until a neutral pH is obtained. After drying the organic phase (MgSO4), filtration on paper and evaporation of the solvents, the residue is chromatographed on a column of silica gel, eluting with an MeOH/CH2Cl2 mixture (0.5/99.5 v/v). 2.44 g of 1,4-dibenzyl-2-tert-butylcarbonylaminomethylpiperazine are thus obtained in the form of a viscous product. Yield: 49%. Rf═0.36 (95/5 v/v CH2Cl2/MeOH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531476B1
Source datasetuspto-grants-2003_03
ORD IDord-b8714528d34e4dab8255c35074052a3c
Source noteuspto-grants-2003_03