HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232541Generated: October 30, 2026
Ethyl bromoacetate → HCID 67713780, compound
https://huagongshe.com/reaction/232541
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Phenylacetophenone | HCID 9948 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Product | HCID 67713780 | HCID 67713780 | — |
Reaction Steps
To a solution of 6.0 g of 60% sodium hydride in 150 ml of THF was added dropwise a solution of 29.4 g of deoxybenzoin in 150 ml THF. The mixture was stirred for 10 min., 16.8 ml of ethylbromoacetate was added dropwise, and the reaction was then heated at reflux under nitrogen overnight. The reaction was then partitioned between ether and 5% aqueous sodium bicarbonate, washed twice with ether dried over magnesium sulfate, filtered and concentrated to 41.08 g of a brown oil. The crude product was mixed with 200 ml of methanol, 30 ml of water and 10 ml of 50% sodium hydroxide and then heated to reflux under nitrogen overnight. After this time the reaction was concentrated, partitioned between water and ether, washed twice with ether and dried over magnesium sulfate. The ether extracts were then concentrated and the residue triturated with cold ether to afford 6.45 gms of a yellow solid, mp 137°-139° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05591729 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-664b5ff32b074601bff2083593e74267 |
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| Source note | uspto-grants-1997_01 |
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