HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzoyl chloride → HCID 23161670, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzoyl chloride | HCID 8501 | — |
| Reactant | 3,5-Dichlorobenzylic alcohol | HCID 43236 | — |
| Reactant | TBDMS ether | HCID 590018 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | HCID 23161670 | HCID 23161670 | — |
Reaction Steps
Compound 26, an intermediate in the preparation of compound 1, can be prepared in several steps beginning with 3,5-dichlorobenzyl alcohol. The alcohol is protected as a t-butyldimethylsilyl ether, then treated with n-butyllithium followed by 4-chlorobenzoyl chloride to produce 4-(t-butyldimethylsilyloxymethyl-2,4',6-trichlorobenzophenone. Removal of the silyl protecting group provides compound 26.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05705514 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-38cadca5dfd348bc8406cdecacda3d5f |
| Source note | uspto-grants-1998_01 |