Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Propanol | HCID 1031 | — |
| Reactant | L-Phenylalanine | HCID 6140 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 13783234 | HCID 13783234 | 99% |
Reaction Steps
A suspension of 2.0 g of L-phenylalanine in 30 ml of n-propyl alcohol was heated to 50° C., 3.5 ml of thionyl chloride added thereto, and the reaction then continued for 5 hours until the L-phenylalanine crystals were dissolved. After completion of the reaction, the mixture was concentrated under a reduced pressure to obtain crude crystals. These crystals were then recrystallized from a solvent mixture of methanol-ether to give 2.93 g of L-phenyl alanine n-propyl ester hydrochloride as colorless crystals (yield: 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05039696 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-4f33f1f0b3c240398deee06d1ed3c02e |
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| Source note | uspto-grants-1991_08 |
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