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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432036Generated: October 31, 2026

Methyl iodide → HCID 86608495, compound

https://huagongshe.com/reaction/1432036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 131727714HCID 131727714—
SolventDimethylformamideHCID 6228—
ProductHCID 86608495HCID 86608495—

Reaction Steps

{[1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-methyl-propyl]-amino}-acetic acid tert-butyl ester (1.9 g, 6.1 mmol) and diisopropylethylamine (4.2 mL, 24 mmol) were dissolved in DMF (15 mL). A solution of MeI (0.45 mL, 7.3 mmol) in DMF (100 mL) was slowly added over 15 min. The reaction was stirred for 2½ h. The solvent was removed in vacuo. The residue product was dissolved in EtOAc (100 mL) and the solution was washed with water (20 mL). The organic phase was dried over magnesium sulfate, filtered and the filtrate was evaporated in vacuo. The residue was dissolved in acetonitrile (45 mL) and Et3N 3HF (2 mL, 12.3 mmol) was added. The reaction was stirred for 16 h. The solvent was removed in vacuo. The crude product was dissolved in EtOAc (100 mL) and washed with saturated sodium bicarbonate solution (25 mL) and saturated sodium chloride solution (25 mL). The organic phase was dried over magnesium sulfate and the solution was slowly filtered through 5 g of silica gel. The filtrate was evaporated in vacuo. Yield: 1.1 g, 78%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612068B2
Source datasetuspto-grants-2009_11
ORD IDord-3dafd75e05bc474d8ed618001091a4a5
Source noteuspto-grants-2009_11