HuagongsheHuagongshe Chemistry Print Report · For research reference only
[4-(2-Chloroethoxy)phenyl](4-hydroxyphenyl)methanone → 4-(2-(Benzo[c][1,2,5]thiadiazol-5-yl)-1-(4-(2-chloro-ethoxy)phenyl)but-1-enyl)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | [4-(2-Chloroethoxy)phenyl](4-hydroxyphenyl)methanone | HCID 89656364 | — |
| Reactant | 1-(Benzo[c][1,2,5]thiadiazol-5-yl)propan-1-one | HCID 89657553 | — |
| Product | 4-(2-(Benzo[c][1,2,5]thiadiazol-5-yl)-1-(4-(2-chloro-ethoxy)phenyl)but-1-enyl)phenol | HCID 136502899 | 10% |
Reaction Steps
According to general procedure of McMurry reaction as example 1, step D described, 1-(benzo[c][1,2,5]thiadiazol-5-yl)propan-1-one (552 mg, 2 mmol) was reacted with (4-(2-chloroethoxy)phenyl)(4-hydroxyphenyl)methanone (384 mg, 2 mmol) to give the desired product (83 mg, 10%, Z/E=1/1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09309211B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-b3c130df9c824efca71603cc5a4148c8 |
| Source note | uspto-grants-2016_04 |