HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 4-(benzyloxy)-3-oxobutanoate → Ethyl 4-benzyloxy-2-[2-(3-cyclopentoxy-4-methoxyphenyl)-2-oxoethyl]-3-oxobutyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 4-(benzyloxy)-3-oxobutanoate | HCID 9813448 | — |
| Reactant | 2-Bromo-1-[3-(cyclopentyloxy)-4-methoxyphenyl]ethan-1-one | HCID 54438505 | — |
| Reactant | 2-Bromo-1-(3-cyclopropylmethoxy-4-difluoromethoxyphenyl)ethanone | HCID 86627052 | — |
| Product | Ethyl 4-benzyloxy-2-[2-(3-cyclopentoxy-4-methoxyphenyl)-2-oxoethyl]-3-oxobutyrate | HCID 66602831 | 75% |
Reaction Steps
Reaction and post treatment were carried out in the same manner as in Reference example 45-(b) except for using 7.65 g (32.4 mmol) of ethyl 4-benzyloxy-3-oxobutyrate in place of ethyl 4-(4-methoxybenzyloxy)-3-oxobutyrate, and using 8.45 g (27 mmol) of 2-bromo-1-(3-cyclopentoxy-4-methoxyphenyl)ethanone obtained in Reference example 47-(a) in place of 2-bromo-1-(3-cyclopropylmethoxy-4-difluoromethoxyphenyl)ethanone, respectively, whereby 9.49 g of the title compound was obtained as a yellowish oil. (Yield: 75%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08450319B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-fe035c19436945dfa90e5ee4a7b933ed |
| Source note | uspto-grants-2013_05 |