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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743794Generated: October 31, 2026

Methyl iodide → HCID 178502718, compound

https://huagongshe.com/reaction/1743794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantPotassium bisulfateHCID 516920—
ReactantHCID 178502721HCID 178502721—
SolventDimethylacetamideHCID 31374—
SolventDiethylether waterHCID 21584184—
ProductHCID 178502718HCID 178502718104.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 95 g (corresponds to 301.26 mmol) of crude trans-[4-(Methoxy-methyl-carbamoyl)-cyclohexylmethyl]-carbamic acid tert-butyl ester in 300 ml of DMA was treated at 0° C. with 19.72 g (451.9 mmol) of NaH (55% in oil) in small portions. The reaction was stirred for 1 h at 0° C., then treated slowly (1.5 h) with 150 ml (2.41 mol) of iodomethane. After the addition of 60 ml of iodomethane (1 h), the reaction started, the addition was stopped and continued after reaction was cooled down again. After warming up to RT over night, the reaction was cooled, neutralized with aqueous 10% KHSO4 and poured into water/Et2O (3×). The organic phase was washed with aqueous 10% NaCl, dried over Na2SO4 evaporated and purified by flash silica gel column (CH2Cl2/EtOAc 9:1 to 1:1) to yield 99 g (quantitative) of trans-[4-(Methoxy-methyl-carbamoyl)-cyclohexylmethyl]-methyl-carbamic acid tert-butyl ester, MS: 315 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012077B2
Source datasetuspto-grants-2006_03
ORD IDord-f5c9495c4eab4723aa1c456f7fd51e6b
Source noteuspto-grants-2006_03