HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855161Generated: October 31, 2026
Methyl iodide → 4-[[(1,1-dimethylethoxy)carbonyl]amino]Butanoic acid methyl ester
https://huagongshe.com/reaction/1855161
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(((Tert-butoxy)carbonyl)amino)butanoic acid | HCID 294894 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-[[(1,1-dimethylethoxy)carbonyl]amino]Butanoic acid methyl ester | HCID 13112352 | 83% |
Reaction Steps
To a solution of 4-(tert-butoxycarbonylamino)butanoic acid (7.0 g, 34.5 mmol) and K2CO3 (9.5 g, 68.9 mmol) in acetone (70 mL) was added MeI (7.5 g, 51.8 mmol) at rt. The reaction solution was stirred at 45° C. for 12 hrs. The mixture was washed with water and saturated sodium chloride, dried over Na2SO4, and concentrated to afford methyl 4-(tert-butoxycarbonylamino)butanoate (6.2 g, 83%) as a yellow oil. ESI-MS (EI+, m/z): 240 [M+Na]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962843B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-9124ed42664640ca8f6717ad8bc9db5a |
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| Source note | uspto-grants-2015_02 |
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