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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118240Generated: October 31, 2026

Methyl iodide → HCID 178476334, compound

https://huagongshe.com/reaction/2118240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178476335HCID 178476335—
SolventDimethylformamideHCID 6228—
ProductHCID 178476334HCID 17847633468.7%

Reaction Steps

To an ice-cooled and stirred solution of the crude 26.0 g trans-acetic acid 4-(2-tert-butoxycarbonylamino-ethyl)-cyclohexylmethyl ester and 5.77 mL (92.6 mmol, 1.1 eq) of CH3I in 300 mL of DMF was added within 15 min 4.04 g (92.58 mmol, 1.1 eq) of NaH (55% in oil). After stirring at RT over night, additional 1.65 mL (26.5 mmol, 0.3 eq) of CH3I and 1.16 g (26.5 mmol, 0.3 eq) of NaH were added and the reaction mixture was then stirred at RT for another 1 h. It was then partitioned between ether, 1M HCl solution and water. The organic layer was dried over MgSO4, concentrated under reduced pressure and the residue was then chromatographed on silica gel with a 4:1 v/v mixture of n-hexane and EtOAc as the eluent giving 18.7 g (68% over 3 steps) of pure trans-acetic acid 4-[2-(tert-butoxycarbonyl-methyl-amino)-ethyl]-cyclohexylmethyl ester as colorless viscous oil, MS: 214 [(M-(tert-butoxycarbonyl))H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442791B2
Source datasetuspto-grants-2008_10
ORD IDord-1dfe8647e402420db9b76fc167820084
Source noteuspto-grants-2008_10