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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446645Generated: October 25, 2026

Trimethylsilyldiazomethane → Methyl 3-[2-(2-{2-[2-(2-iodoacetylamino)ethoxy]ethoxy}ethoxy)ethoxy]propanoate

https://huagongshe.com/reaction/446645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantSodium BicarbonateHCID 516892—
ReactantIodoacetic acid N-hydroxysuccinimide esterHCID 3299230—
ReactantAmino-PEG4-acidHCID 22731902—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
ProductMethyl 3-[2-(2-{2-[2-(2-iodoacetylamino)ethoxy]ethoxy}ethoxy)ethoxy]propanoateHCID 86671288—

Reaction Conditions

Temperature0 °C

Reaction Steps

117.4 mg of N-hydroxysuccinimidyl iodoacetate in solution in 3 ml of DCM are added to 100 mg of 3-(2-{2-[2-(2-aminoethoxy)ethoxy]ethoxy}ethoxy)propanoic acid. After 2 h at AT, 330 μl of MeOH are added and the mixture is cooled to 0° C. 360 μl of a 2M solution of trimethylsilyldiazomethane in hexane are added. After 1 h, the mixture is neutralized by addition of 50 μl of acetic acid and then a saturated aqueous NaHCO3 solution is added until pH=8 is obtained. The organic phase is dried over MgSO4 and concentrated under RP, and the residue is purified by flash chromatography on silica (Interchrom Puriflash Silica 15/35U 10G) using a gradient from 0 to 10% of methanol in DCM. 132 mg of methyl 3-[2-(2-{2-[2-(2-iodoacetylamino)ethoxy]ethoxy}ethoxy)ethoxy]propanoate are thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481042B2
Source datasetuspto-grants-2013_07
ORD IDord-502cb843f07243369ff56202f0bbb50d
Source noteuspto-grants-2013_07