HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393697Generated: October 29, 2026
Ammonium Chloride → 4-(R)-Benzyl-3-(2-(R)-hydroxymethyl-3-methylbutyryl)oxazolidin-2one
https://huagongshe.com/reaction/393697
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (4R)-4-Benzyl-3-(3-methylbutanoyl)-1,3-oxazolidin-2-one | HCID 11391340 | — |
| Reactant | CID 19593658 | HCID 19593658 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(R)-Benzyl-3-(2-(R)-hydroxymethyl-3-methylbutyryl)oxazolidin-2one | HCID 22888285 | 124.2% |
Reaction Steps
Titanium tetrachloride (18 ml) was added dropwise to a solution of 4-(R)-benzyl-3-(3-methylbutanoyl)oxazolidin-2-one (41.5 g) in dichloromethane (300 ml) at 0° C. Diisopropylethylamine (28 ml) was added dropwise and the resulting purple suspension was stirred for 30 min, then a solution of trioxane (11.2 g) was added, followed by titanium tetrachloride (18 ml) and the mixture was stirred for two hours, during which time the solution changed in colour from purple to amber. Ammonium chloride (400 ml saturated aqueous solution) was added and the mixture was stirred for 10 min, then the phases separated and the organic layer washed with water and saturated brine, dried (Na2SO4) and evaporated to give the title compound as a colourless solid (45 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06809100B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-ceb2541d29d7425a83902bb9986d00b8 |
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| Source note | uspto-grants-2004_10 |
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