HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037358Generated: November 1, 2026
alpha-Chlorohydrin, (+)- → HCID 68628850, compound
https://huagongshe.com/reaction/2037358
Participants
| Role | Name | HCID | Charge |
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| Reactant | alpha-Chlorohydrin, (+)- | HCID 148904 | — |
| Reactant | HCID 136344049 | HCID 136344049 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 68628850 | HCID 68628850 | 32.4% |
Reaction Steps
To a solution of 2-ethyl-4-[5-(4-isobutyl-6-methyl-pyridin-2-yl)-[1,2,4]oxadiazol-3-yl]-6-methyl-phenol (41 mg, 0.116 mmol) in isopropanol (3 mL) and 3 N aq. NaOH (0.4 mL), (S)-3-chloro-1,2-propanediol (66 mg, 0.577 mmol) is added. The mixture is stirred at 65° C. for 16 h before another portion of (S)-3-chloro-1,2-propanediol (66 mg, 0.577 mmol) and 3 N aq. NaOH (0.4 mL) is added. Stirring is continued at 65° C. for 24 h. The mixture is cooled to rt, diluted with water, and repeatedly extracted with diethyl ether. The combined org. extracts are dried over MgSO4, filtered and concentrated. The crude product is purified on prep. TLC using DCM:methanol 9:1 to give the title compound (16 mg) as a colourless oil; LC-MS: tR=1.02 min, [M+H]+=426.17.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08575200B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-2dd74b0199bf4e3fbdc27bc1e0d47b7f |
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| Source note | uspto-grants-2013_11 |
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