Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (2R)-4-AMINO-2-HYDROXYBUTYRIC ACID | HCID 5287507 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54281127 | HCID 54281127 | — |
Reaction Steps
17.2 g of p-methoxybenzoyl chloride are added while stirring well to 6.0 g of (R)-4-amino-2-hydroxy-butyric acid and 150 ml of ion-free water. The mixture is then adjusted to pH 10.5 with 2 N sodium hydroxide and stirred at room temperature for 70 minutes. The clear solution is treated with ice and adjusted to pH 1.4 with 25% hydrochloric acid. The separated solid is filtered off and washed with water. The filtrate is adjusted to pH 5.5 with sodium hydroxide and concentrated in a water-jet vacuum. The clear colourless solution is adjusted to pH 1.4 with 25% hydrochloric acid and extracted firstly with ether and then with ethyl acetate. The aqueous phases are adjusted to pH 5.5, concentrated, acidified with 25% hydrochloric acid and extracted with ethyl acetate. The combined ethyl acetate extracts are evaporated and the residue is recrystallised from ethyl acetate. There is obtained (R)-4-(p-methoxybenzoylamino)-2-hydroxy-butyric acid of melting point 105°-106° C.; [α]D20 = -12.4°; [α]36520 =-60.5° (c=1.0 in water). A further amount of (R)-4-(p-methoxybenzoylamino)-2-hydroxy-butyric acid of melting point 103.5°-104.5° C. can be isolated from the mother liquors.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04461906 |
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| Source dataset | uspto-grants-1984_07 |
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| ORD ID | ord-d2a39b71d08545c1af68f34e9d04fdf6 |
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| Source note | uspto-grants-1984_07 |
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