HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylbenzyl chloride → HCID 19792563, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylbenzyl chloride | HCID 7722 | — |
| Reactant | Acetylacetone | HCID 31261 | — |
| Product | HCID 19792563 | HCID 19792563 | — |
Reaction Steps
Using 2,4-pentandione (195.2 g, 1.95 moles) and 4-methylbenzylchloride (635.4 g), the reaction was carried out in the same manner as described in Example 17, (1), and the residue (568 g) was recrystallized from ethanol to afford the title compound as a white needles which was an ca 1:9 mixture of Keto/Enol as seen by the methylene singlet at δ3.50 ppm and the methine singlet at δ5.43 ppm in the 1HNMR spectrum; yield: 155 g; mp 74.8°-75.7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05250669 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-2bf3b9640ac84fcf8402ea3794ce5f70 |
| Source note | uspto-grants-1993_10 |