HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1080505Generated: October 25, 2026
Hydrochloric Acid → N-[1(S)-benzyl-3-hydroxy-2-oxopropyl]phthalimide
https://huagongshe.com/reaction/1080505
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | (Vinyl-2-ylidenetris(oxy))tris(trimethylsilane) | HCID 553067 | — |
| Reactant | 3-phenyl-2(S)-phthalimidopropionyl chloride | HCID 10567197 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-[1(S)-benzyl-3-hydroxy-2-oxopropyl]phthalimide | HCID 10267319 | 78% |
Reaction Steps
A mixture of 134 g of 3-phenyl-2(S)-phthalimido-propionyl chloride and 269.7 g of tris(trimethylsilyloxy)-ethylene was stirred at 95° C. for 5 hours. A further 54 g of tris(trimethylsilyloxy)ethylene were added and the mixture was stirred at 95° C. for a further 1.5 hours. The cooled reaction mixture was then treated with 435 ml of dioxan and 174 ml of 0.6N hydrochloric acid and the resulting mixture was heated to 85° C. for 30 minutes. The cooled mixture was saturated with sodium chloride and then extracted with diethyl ether. The ethereal solution was washed with aqueous sodium bicarbonate solution and evaporated. The resulting pale yellow solid was crystallized from ethyl acetate/n-hexane to give 103 g of N-[1(S)-benzyl-3-hydroxy-2-oxopropyl]phthalimide as a white solid, MS: m/e 310 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05580999 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-b79cc8c7dcdb49b29f92959c90a943f2 |
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| Source note | uspto-grants-1996_12 |
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