HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065915Generated: November 3, 2026
alpha-Chlorohydrin, (+)- → HCID 59392504, compound
https://huagongshe.com/reaction/2065915
Participants
| Role | Name | HCID | Charge |
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| Reactant | alpha-Chlorohydrin, (+)- | HCID 148904 | — |
| Reactant | HCID 136170273 | HCID 136170273 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 59392504 | HCID 59392504 | 11.5% |
Reaction Steps
To a solution of 4-[5-(5,6-diethyl-pyridin-3-yl)-[1,2,4]oxadiazol-3-yl]-2-ethyl-6-methyl-phenol (100 mg, 0.296 mmol) in isopropanol (10 mL) and 3 N aq. NaOH (3 mL), (S)-3-chloro-1,2-propanediol (98 mg, 0.89 mmol) is added. The mixture is stirred at 60° C. for 24 h before another portion of (S)-3-chloro-1,2-propanediol (98 mg, 0.89 mmol) is added. Stirring is continued at 60° C. for 2 days. The mixture is diluted with EA and washed with sat. aq. NaHCO3 solution. The org. extract is dried over MgSO4, filtered and evaporated. The crude product is purified by chromatography on prep. TLC plates with EA-heptane to give (S)-3-{4-[5-(5,6-diethyl-pyridin-3-yl)-[1,2,4]oxadiazol-3-yl]-2-ethyl-6-methyl-phenoxy}-propane-1,2-diol (14 mg) as a red oil; LC-MS: tR=0.93 min, [M+1]+=412.16.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08288554B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-be66c2f7874947428716cb5b866a8d1e |
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| Source note | uspto-grants-2012_10 |
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