HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74115Generated: October 28, 2026
Hydrochloric Acid → (2R)-2-Amino-3-hydroxy-N-(phenylmethyl)propanamide
https://huagongshe.com/reaction/74115
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | tert-butyl N-[(1R)-1-(benzylcarbamoyl)-2-hydroxyethyl]carbamate | HCID 46223140 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2R)-2-Amino-3-hydroxy-N-(phenylmethyl)propanamide | HCID 10655432 | 73.52% |
Reaction Steps
To a 500 mL four-neck round bottom flask, 34.0 g (R)-N-benzyl-2-(tert-butoxycarbonylamino)-3-hydroxypropionamide and 350 mL dichloromethane were added, and the mixture was stirred to obtain a clear solution. At 20-25° C., 40.0 g concentrated hydrochloric acid (having a mass concentration of 36.0%) was added, and the reaction was continued. TLC tracking was performed, till the raw materials were completely converted. After the reaction was completed, the temperature was decreased to 20° C. The mixture was suction-filtered, to obtain a white needle-like crystal. The obtained white crystalline solid was dissolved in 50 g water. At 20-25° C., 30% sodium hydroxide solution was added to adjust the pH value of the system to 8-9. After the addition, the solution was stirred continuously, and a white flaky crystal was precipitated. The mixture was suction-filtered, and the filter was washed and dried, to obtain a target product of 16.5 g (0.085 mol). The molar yield was 73.52%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829226B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-2fc6ac5f6b8c4ae491efb78357efebdf |
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| Source note | uspto-grants-2014_09 |
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