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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294719Generated: October 31, 2026

Methyl iodide → HCID 86751654, compound

https://huagongshe.com/reaction/2294719

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86751653HCID 86751653—
SolventAcetoneHCID 180—
ProductHCID 86751654HCID 86751654—

Reaction Steps

A mixture of 1.1 g (2.43 mmol) of 4-benzyl 1-tert-butyl N-[(1-tert-butoxyformamido)thioacetyl]-L-aspartate, 1.95 ml of methyl iodide and 0.92 g of potassium carbonate in 50 ml of acetone is stirred at room temperature overnight. Thereafter, the solvent is distilled off under reduced pressure and the residue is taken up in ether. The organic phase is washed with water, dried over sodium sulphate and evaporated. 4-Benzyl 1-tert-butyl N-[2-(1-tert-butoxyformamido)-1-(methylthio)ethylidene]-L-aspartate is obtained as a mixture of the E- and Z-isomers; MS: 467 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05688946
Source datasetuspto-grants-1997_11
ORD IDord-23b188f611e349828e16c81d14b32d2e
Source noteuspto-grants-1997_11