HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254528Generated: October 31, 2026
Trifluoroacetic acid → L-Valyl-N-Methyl-L-Alanyl-L-Alanine Benzyl Ester
https://huagongshe.com/reaction/2254528
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Boc-L-Valyl-N-Mehtyl-L-Alanyl-L-Alanine Benzyl Ester | HCID 14673106 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | L-Valyl-N-Methyl-L-Alanyl-L-Alanine Benzyl Ester | HCID 14673108 | — |
Reaction Steps
A stirred solution of 17 g (0.0367 mole) Boc-L-valyl-N-methyl-L-alanyl-L-alanine benzyl ester in 170 ml of dry dichloromethane was cooled at -10° C. as 85 ml of trifluoroacetic acid, previously cooled at -15° C., was added. After 16 hours at -5° C., the reaction was carefully poured with good stirring into a mixture of 93 g of sodium bicarbonate, ice, and 250 ml of dichloromethane. The organic layer was separated and the aqueous layer was extracted with another 75 ml of dichloromethane. The combined organic layers were washed with 3×75 ml of saturated sodium bicarbonate solution, dried over magnesium sulfate, and evaporated to give 12.8 g (96% of theory) of crude product which was used in step 5 without further purification. FAB m.s. showed a molecular ion peak at 364.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05236899 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-b21d5bef50904eb5b4b794507c6b6a37 |
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| Source note | uspto-grants-1993_08 |
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