HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Acetoxy-2-bromoethane → Ethyl 4'-(2-acetoxyethoxy)-3-bromobiphenyl-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Acetoxy-2-bromoethane | HCID 13564 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 3'-bromo-4'-hydroxybiphenyl-4-carboxylate | HCID 16657517 | — |
| Reactant | Ethyl 4'-(2-acetoxyethoxy)-3'-bromobiphenyl-4-carboxylate | HCID 66672003 | — |
| Product | Ethyl 4'-(2-acetoxyethoxy)-3-bromobiphenyl-4-carboxylate | HCID 68643383 | 95% |
Reaction Steps
In a manner similar to that of Example 6a, by reacting 2 g (6 mmol) of ethyl 3′-bromo-4′-hydroxybiphenyl-4-carboxylate with 320 mg (8 mmol) of 60% sodium hydride and 0.7 mL (7 mmol) 2-bromoethan-1-ol acetate, 2.2 g of ethyl 4′-(2-acetoxyethoxy)-3′-bromobiphenyl-4-carboxylate are obtained (yield=95%) in the form of a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07807708B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-2b8ca49e6b084eb59f26cbce2e2ab0ef |
| Source note | uspto-grants-2010_10 |