HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetylacetone → HCID 10149969, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetylacetone | HCID 31261 | — |
| Reactant | 4-Methyloxybenzyl chloride | HCID 69993 | — |
| Product | HCID 10149969 | HCID 10149969 | — |
Reaction Steps
Using 2,4-pentanedione (37.3 g, 0.37 mol) and 4-methoxybenzyl chloride (133 g), the reaction was carried out in the same manner as described in Example 17, (1), and the solid residue was purified by recrystalization from ethanol to give the title compound as pale yellow microneedles which were not shown any methylene singlet at δ3.0-4.0 ppm in the 1HNMR spectrum; yield: 95.1 g; mp 73.5°-76.2° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05250669 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-b0a87b969e0c4400ac0118afa352bbf7 |
| Source note | uspto-grants-1993_10 |