HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342626Generated: October 25, 2026
Potassium bisulfate → tert-butyl N-[(2S)-1-oxo-3-phenylpropan-2-yl]carbamate
https://huagongshe.com/reaction/342626
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | 1,1-Dimethylethyl N-((1S)-2-(methoxymethylamino)-2-oxo-1-(phenylmethyl)ethyl)carbamate | HCID 11055945 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | tert-butyl N-[(2S)-1-oxo-3-phenylpropan-2-yl]carbamate | HCID 6998013 | — |
Reaction Steps
A mechanically stirred suspension of lithium aluminum hydride (6.59 g, 0.165 mol) in ether (1 L) was cooled to -45° C. under nitrogen. A solution of the product from Step A (0.150 mol) in ether (150 mL) was added, maintaining the temperature below -35° C. When the addition was complete, the reaction was warmed to 5° C., then recooled to -45° C. A solution of potassium hydrogen sulfate (36.1 g, 0.265 mol) in water was slowly added, maintaining the temperature below -5° C. After quenching, the reaction was stirred at room temperature for 1 h. The mixture was filtered through Celite, the ether evaporated, and the remainder partitioned between ethyl acetate and 2% potassium hydrogen sulfate. After washing with saturated brine, drying over magnesium sulfate and solvent removal, the title compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05859012 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-9076447184b9488f8a35983007bd93a5 |
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| Source note | uspto-grants-1999_01 |
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