HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404945Generated: October 31, 2026
Hydrochloric Acid → HCID 10488616, compound
https://huagongshe.com/reaction/404945
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diphenyl carbonate | HCID 7597 | — |
| Reactant | HCID 67178178 | HCID 67178178 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 10488616 | HCID 10488616 | — |
Reaction Steps
Under a nitrogen atmosphere, 428 mg (2 mmol) of diphenyl carbonate and 5 mL of acetonitrile were loaded into a round bottom flask having a volume of 100 mL, and then the mixture was stirred at room temperature. Next, 847 mg (2 mmol) of tetrabutylphosphonium phenylalanine salt and 15 mL of acetonitrile were dropped to the solution, and then the mixture was stirred for 15 minutes. After that, a 1M aqueous HCl solution was added to the reaction solution to terminate the reaction, and then the resultant was concentrated with an evaporator. Next, water was added to the concentrated product, and then the resultant was extracted with ethyl acetate. The resultant organic layer was washed with water and brine, and was then dried with sodium sulfate. After that, the dried product was concentrated with an evaporator. Thus, a crude product was obtained. Next, the crude product was purified by column chromatography. Thus, N-phenoxycarbonyl-L-alanine was obtained. An isolation amount and an isolation yield were 416.6 mg and 73%, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08748650B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-e3efb64342cc46f3a05e1cee19cba58b |
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| Source note | uspto-grants-2014_06 |
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