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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Iodoacetic acid N-hydroxysuccinimide ester | HCID 3299230 | — |
| Reactant | Amino-PEG4-acid | HCID 22731902 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Methyl 3-[2-(2-{2-[2-(2-iodoacetylamino)ethoxy]ethoxy}ethoxy)ethoxy]propanoate | HCID 86671288 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481042B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-502cb843f07243369ff56202f0bbb50d |
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| Source note | uspto-grants-2013_07 |
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