HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249193Generated: October 29, 2026
N-(2-aminoethyl)acetamide → HCID 14235033, compound
https://huagongshe.com/reaction/2249193
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-(2-aminoethyl)acetamide | HCID 66082 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | Tetrahydro-2,5-dimethoxyfuran-3-carbaldehyde | HCID 567310 | — |
| Product | HCID 14235033 | HCID 14235033 | — |
Reaction Steps
8.5 g (0.053 mol) of 2,5-dimethoxytetrahydrofuran-3-aldehyde and 5.4 g (0.053 mol) of 2-(acetylamino)-ethylamine are stirred at 60° C. for 1 hour. After addition of 0.05 g of p-toluenesulphonic acid hydrate, the mixture is stirred at 80° C. for 90 minutes and cooled, sodium bicarbonate solution is added and the mixture is extracted with methylene chloride and then with pentanol. The organic phases are concentrated and chromatographed over a silica gel column with methylene chloride/methanol =95:5 as the mobile phase. The product isolated is crystallized from ethyl acetate/ligroin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05043348 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-e28a67eca1594495bf06308bf10995c0 |
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| Source note | uspto-grants-1991_08 |
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