HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072755Generated: October 31, 2026
Trifluoroacetic acid → N-Methyl-L-Alanyl-L-Alanine benzyl Ester
https://huagongshe.com/reaction/2072755
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Benzyl (S)-2-[(S)-2-(tert-butoxycarbonyl-methyl-amino)-propanoylamino]-propionate | HCID 14673102 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-Methyl-L-Alanyl-L-Alanine benzyl Ester | HCID 14673104 | — |
Reaction Steps
To a stirred solution of 17 g (0.0466 mole) of Boc-N-methyl-L-alanyl-L-alanine benzyl ester in 150 ml of dry dichloromethane, cooled at -10° C., was added 100 ml trifluoroacetic acid, which was previously cooled at -10° C. The reaction mixture was stirred for 16 hours at -5° C., then poured carefully with good stirring into a mixture of 177 g of sodium bicarbonate, ice, and 150 ml of dichloromethane. The organic layer was separated and the aqueous layer was further extracted with another 60 ml of dichloromethane. The combined organic layers were washed with 3×50 ml of saturated sodium bicarbonate solution, dried over manesium sulfate, and evaporated to give 11.6 g (91% of theory) of crude product which was used in step 3 without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04914188 |
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| Source dataset | uspto-grants-1990_04 |
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| ORD ID | ord-9d11f8451d2b4cf59e56b9c9ca5c76c8 |
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| Source note | uspto-grants-1990_04 |
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