HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930375Generated: October 31, 2026
Lithium hydroxide, monohydrate → HCID 66729176, compound
https://huagongshe.com/reaction/1930375
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | HCID 66728977 | HCID 66728977 | — |
| Solvent | Ethanol tetrahydrofuran water | HCID 18504229 | — |
| Product | HCID 66729176 | HCID 66729176 | 46% |
Reaction Steps
To a stirring suspension of ethyl 2-tert-butyl-4-morpholinopyrimidine-5-carboxylate (0.36 g, 1.24 mmol) in 1:1:1 THF/EtOH/H2O (9 ml) at RT was added LiOH—H2O (130 mg, 4.95 mmol) and the mixture was stirred overnight at RT. The reaction mixture was checked by LC-MS and the completed reaction was concentrated to an aqueous residue, acidified (pH 3-4) with 3M HCl and the solution was extracted with EtOAc (3×). The combined organics were washed with brine (1×), dried (MgSO4), filtered and concentration. The crude was dissolved in isopropanol and the solid (LiCl and NaCl) was filtered and washed with isopropanol. The filtrate was concentrated to obtain the desired product 2-tert-butyl-4-morpholinopyrimidine-5-carboxylic acid (0.15 g, 46% yield). MS (ESI) m/z: 266.0 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188113B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-eb62b9c0543a4b68b29b1f96eb0c44aa |
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| Source note | uspto-grants-2012_05 |
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