HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197652Generated: October 29, 2026
2,2-Dimethoxypropane → HCID 68972378, compound
https://huagongshe.com/reaction/2197652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2-Dimethoxypropane | HCID 6495 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | HCID 10084124 | HCID 10084124 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 68972378 | HCID 68972378 | — |
Reaction Steps
(1S,2S)-(2-hydroxy-1-phenyl-but-3-enyl)carbamic acid t-butyl ester is dissolved in an aromatic solvent. 2,2-Dimethoxypropane is added at a temperature in the range of about 20-40° C. followed by addition of pyridinium p-toluene sulfonate. The reaction mixture is heated to about 70-95° C. and stirred at the same temperature for about 1-5 hours. The reaction mixture is cooled to about 30 to 45° C., neutralized with pyridine, and concentrated under reduced pressure to get (4S,5R)-2,2-dimethyl-4-phenyl-5-vinyl-oxazolidine-3-carboxylic acid t-butyl ester in a semi solid form, which is optionally further purified by column chromatography, such as using petroleum ether and ethyl acetate as solvents.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338617B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-856254cedeea4682a89779015aa5e54e |
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| Source note | uspto-grants-2012_12 |
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