Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminopropanol | HCID 5126 | — |
| Reactant | Ethyl Lactate | HCID 7344 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86099196 | HCID 86099196 | — |
Reaction Steps
3.7 g ethyl lactate and 2.1 g 2-amino-1-propanol were mixed and subsequently heated to 110-115° C. for 2.5 hours. During the reaction, the ethanol formed was distilled off. After the reaction the excess of ethyl lactate was removed by vacuum distillation (bottom temperature: 150° C., 1 mbar), using a 20 cm vigreux column. 3.9 g of residual N-lactoyl 2-amino-1-propanol (brown viscous liquid) was collected, the purity of which was confirmed by NMR analysis. The yield of the reaction was 95%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09155329B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-2ab2a64603c744e28c7ac545f97b9dad |
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| Source note | uspto-grants-2015_10 |
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