HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl acetoacetate → 5-Methyl-1-phenylhexan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Methyl-1-phenylhexan-1-one | HCID 570692 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 5-Methyl-1-phenylhexan-1-one | HCID 570692 | — |
| Product | HCID 54703398 | HCID 54703398 | — |
Reaction Steps
The title compound was prepared as described in General Method 1 using 14.2 mmol of methyl acetoacetate, 15.6 mmol of NaH 60% dispersion in oil, 14.9 mmol of 1.6M n-butyl lithium in hexane, 14.2 mmol of isoheptanophenone and 50 mL of tetrahydrofuran. Isoheptanophenone was prepared by reacting the appropriate acid chloride with AlCl3 in benzene as described by Vogel in Practical Organic Chemistry 1978, 770-775. Upon concentrating the reaction, a solid precipitated out which was recrystallized from ethyl acetate (m.p. 124°-125° C.). 1H NMR (CDCl3) δ 0.80 (d,d, 6 H), 1.1-1.2 (m, 2 H), 1.15-1.40 (m, 2 H), 1.4-1.5 (m, 1 H), 1.9-2.0 (m, 2 H), 2.88 (d, 1 H), 2.9 (d, 1 H), 3.2 (d, 1 H), 3.3 (d, 1 H), 7.2-7.5 (m, 5 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05840751 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-2463a4b90ae54c659724009081d58b07 |
| Source note | uspto-grants-1998_11 |