HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857716Generated: October 27, 2026
Ethyl Acetate → 2-benzyloxy-N-methyl-N-(3-methyl-2-oxobutyl)acetamide
https://huagongshe.com/reaction/1857716
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Benzyloxyacetyl chloride | HCID 177085 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Methyl-1-(methylamino)butan-2-one | HCID 22130554 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-benzyloxy-N-methyl-N-(3-methyl-2-oxobutyl)acetamide | HCID 22130912 | 42% |
Reaction Steps
A mixture of 6.1 g (52.9 mmol) of 3-methyl-1-methylamino-2-butanone, 70.0 ml of ethyl acetate and 41.0 ml of water was stirred at 0° C. Added was 7.1 g (84.6 mmol) of sodium hydrogen carbonate, and the mixture was stirred for 10 minutes. There was added 8.5 ml (54.0 mmol) of benzyloxyacetylchloride over 30 minutes. After stirring at room temperature for 10 hours, the ethyl acetate layer was seperated, washed with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The crude product was purified by silica gel chromatography (hexane/ethyl acetate 1:1) to give 5.8 g of 2-benzyloxy-N-methyl-N-(3-methyl-2-oxobutyl)-acetamide (18a') (yield 42%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06147097 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-90bd613fa49943bfbe4bf0929ac19370 |
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| Source note | uspto-grants-2000_11 |
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