HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995105Generated: October 27, 2026
Phenethyl bromide → Tert-butyl 3-oxo-2-phenethylbutanoate
https://huagongshe.com/reaction/1995105
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Tert-butyl acetoacetate | HCID 15538 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Tert-butyl 3-oxo-2-phenethylbutanoate | HCID 13195717 | — |
Reaction Steps
Sodium (2.3 g; 0.10 mol) was allowed to react with dry ethanol (50 ml) under nitrogen. The resulting clear solution was cooled (ice bath) and t-butyl acetoacetate (15.8 g; 0.10 mol) was added during 10 minutes with stirring. After 10 minutes, 2-(bromoethyl)benzene (18.5 g; 0.10 mol) was added during 30 minutes. The resulting solution was heated at reflux for 4 hours, then cooled and filtered. After concentration, the residue was partitioned between water and ether, and the ether layer was dried (MgSO4) and concentrated. Distillation of the residue gave 21.0 g (0.080 mol; 80%) of the title product; bp 110°-120° (0.3 mm). NMR (CDCL3); 1.45 (9H,s), 2.17 (3H,s), 1.8-2.4 (2H,m), 2.5-2.7 (2H,m); 3.28 (1H,J=7); 7.2-7.4 (5H, broad s). MS (m/e); 262 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04402969 |
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| Source dataset | uspto-grants-1983_09 |
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| ORD ID | ord-b621a161861b44cebe0a0054a1713501 |
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| Source note | uspto-grants-1983_09 |
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