HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594448Generated: October 26, 2026
Pyridine → Methyl 4-triphenylmethyloxy-3-hydroxybutyrate
https://huagongshe.com/reaction/1594448
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Methyl 3,4-dihydroxybutanoate | HCID 2735094 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 4-triphenylmethyloxy-3-hydroxybutyrate | HCID 11245840 | 26.8% |
Reaction Steps
To 25 g of methyl 3,4-dihydroxybutanoate was added 250 mL of DCM and stirred to dissolve. 19.8 g of pyridine was added and cooled to 0° C. 41.4 g of trityl chloride was dissolved in 50 mL of DMC and was added at 0-5° C. for 15 minutes. The temperature was allowed to rise to room temperature and was stirred at room temperature for 17 hours. Water was added and the layers were separated. The organic layer was washed with brine, dried and concentrated. The residue was triturated with 25 mL of cyclohexane and the product was purified to give 15 g of the pure product. 1H NMR (CDCl3): 4.25 (m, 1H), 3.6 (s, 3H), 3.15 (d, 2H), 2.5 (m, 2H), 7.2-7.4 (m, 15H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07301046B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-aebd074fa0174b8eb8f45f0d9731dd14 |
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| Source note | uspto-grants-2007_11 |
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