HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395809Generated: October 30, 2026
4-Methylmorpholine → t-Butoxycarbonylvalyltyrosine methyl ester
https://huagongshe.com/reaction/1395809
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | Methyl tyrosinate hydrochloride | HCID 76956 | — |
| Reactant | Boc-L-Valine | HCID 83693 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | t-Butoxycarbonylvalyltyrosine methyl ester | HCID 14752398 | — |
Reaction Steps
21.7 g of t-butoxycarbonylvaline is dissolved in 200 ml of methylene chloride. 22.2 ml of N-methylmorpholine is added to the solution. The solution is cooled to -70° C. 13.1 ml of isobutylchloroformate is then added. The reaction mixture is again cooled to -70° C. 23.2 g of tyrosine methyl ester hydrochloride is added to the reaction mixture. The reaction mixture is allowed to warm to room temperature, and then is stirred for 16 hours. The reaction mixture is extracted three times with 0.5 M potassium bisulfate and once with brine. The methylene chloride solution is dried over anhydrous sodium sulfate, filtered and stripped of solvent. The residue is dissolved in 200 ml of ethyl ether. The ether solution is added to cold rapidly stirring Skellysolve B. The white precipitate is filtered and dried to afford the product t-butoxycarbonylvalyltyrosine methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04204991 |
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| Source dataset | uspto-grants-1980_05 |
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| ORD ID | ord-2273e8eb9ebd41a58e68eaeaf23ea4ac |
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| Source note | uspto-grants-1980_05 |
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