HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromobenzaldehyde → HCID 19817991, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromobenzaldehyde | HCID 76583 | — |
| Reactant | HCID 15617421 | HCID 15617421 | — |
| Product | HCID 19817991 | HCID 19817991 | — |
Reaction Steps
Similarly, following the procedure of Example 7(b), 3-bromobenzaldehyde was reacted with 1-phenylocta-1,7-diyne to yield 3-(8-phenyl-1,7-octadiynyl)benzaldehyde which was reduced to 3-(8-phenyloctyl)benzaldehyde and the latter was reacted as described in Example 35(a), (b) and (c) to give 3-(2-carboxyethylthio)-3-[3-(8-phenyloctyl)phenyl]-2-hydroxypropanoic acid, dipotassium salt, hydrate as a mixture of isomers, -log KB value 6.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04820719 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-4e9243d253bf438586fd3baabb92ae54 |
| Source note | uspto-grants-1989_04 |