HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269652Generated: October 29, 2026
Methyl iodide → (2S,3R)-2-{[(tert-butoxy)carbonyl]amino}-3-methoxybutanoic acid
https://huagongshe.com/reaction/2269652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-tert-Butoxycarbonyl-L-threonine | HCID 2724766 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2S,3R)-2-{[(tert-butoxy)carbonyl]amino}-3-methoxybutanoic acid | HCID 15460346 | — |
Reaction Steps
In a THF solution containing 0.8 g of Boc-Thr-OH, 100 mg of sodium hydride (60% in oil) was added under ice cooling and the resultant mixture was stirred for 30 min at room temperature. Further, 2.8 ml of methyl iodide was added and the obtained reaction mixture was stirred overnight at room temperature. The reaction mixture was evaporated under reduced pressure and the resultant residue was redissolved in ethyl acetate, washed with 5% sodium hydrogensulfite aqueous solution, water and saturated sodium chloride aqueous solution, successively, and dried over anhydrous sodium sulfate. The dried solution was evaporated under reduced pressure, dissolved in methanol, mixed with DCHA and reevaporated. Ether-hexane was added to the residue to give 0.55 g of the title compound as its DCHA salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06329502B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-483e46cf61b245a5b5bdde046e4289ca |
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| Source note | uspto-grants-2001_12 |
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