HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814818Generated: October 25, 2026
DL-alanine → 2-(2-Ethyl)octanoylaminopropionic acid
https://huagongshe.com/reaction/1814818
Participants
| Role | Name | HCID | Charge |
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| Reactant | DL-alanine | HCID 602 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Ethyloctanoyl chloride | HCID 14597158 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(2-Ethyl)octanoylaminopropionic acid | HCID 21973174 | — |
Reaction Steps
18.6 g (0.211 mol) of D,L-alanine and 46.6 g (0.41 mol) of triethylamine are initially charged in 300 ml of dichloromethane. At 0° C., 50.09 g (0.461 mol) of trimethylsilyl chloride are added dropwise, and the mixture is stirred at room temperature for 1 h and then at 40° C. for 1 h. The solution is cooled to −10° C., and 40 g (0.21 mol) of 2-ethyloctanoyl chloride in 50 ml of dichloromethane are added dropwise. The mixture is stirred at room temperature overnight, 100 ml of water are then added dropwise with ice-cooling and the mixture is stirred for 10 minutes. The phases are separated, the aqueous phase is reextracted twice with in each case 100 ml of dichloromethane and the combined organic phases are dried over sodium sulfate and concentrated under reduced pressure. The residue is crystallized from toluene by adding n-hexane and is dried at 60° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06878708B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-6ab3de7519ef4352a8c38551ead32eed |
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| Source note | uspto-grants-2005_04 |
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