HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245410Generated: November 3, 2026
Hydrochloric Acid → (R)-4-Benzyl-3-morpholinecarboxylic acid
https://huagongshe.com/reaction/2245410
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | (R)-Ethyl 4-benzylmorpholine-3-carboxylate | HCID 13543384 | — |
| Solvent | Ethanol tetrahydrofuran water | HCID 18504229 | — |
| Product | (R)-4-Benzyl-3-morpholinecarboxylic acid | HCID 1514260 | 94% |
Reaction Steps
Ethyl (3R)-4-(phenylmethyl)-3-morpholinecarboxylate (D46, 2.33 g, 9.36 mmol) was dissolved in a mixture of THF/EtOH/H2O (1:1:1 45 mL) before treating with Lithium Hydroxide monohydrate (0.432 g, 10.29 mmol) and heating at 50° C. overnight. Reaction not finished. Added more Lithium Hydroxide monohydrate (0.200 g, 4.76 mmol) and left heating for a further 24 hours. Added more Lithium Hydroxide (0.100 g, 2.38 mmol) and heated for a further 6 hours. Added more Lithium Hydroxide (0.100 g, 2.38 mmol) and heated for a further 16 hours. Cooled to R.T. Reaction neutralised using 2N HCl solution. Solvent evaporated. Residue partitioned between DCM and Water. Aqueous layer extracted with 10% MeOH/DCM ×5. Combined extracts dried (MgSO4). Filtered. Solvent evaporated under reduced pressure to afford the title compound as a white foam in a 94% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07683056B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-9dd8dce42d2a44c8a245854a309c034b |
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| Source note | uspto-grants-2010_03 |
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