HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → Biphenyl-2,2'-diyl diethyl dicarbonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | (1,1'-Biphenyl)-2,2'-diol | HCID 15731 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Biphenyl-2,2'-diyl diethyl dicarbonate | HCID 58288702 | — |
Reaction Steps
To a round-bottom flask is charged biphenyl-2,2′-diol (7.45 g, 40 mmol) and pyridine (50 mL). The flask is immersed in an ice-water bath and ethyl chloroformate (9.48 mL, 100 mmol) is added dropwise. After gradually warming to room temperature, the mixture is stirred overnight. The volatiles are removed in vacuo, and the residue is suspended in 100 mL of ethyl acetate. After filtration, the filtrate is concentrated and purified by flash chromatography. The product is obtained as a colorless oil. Yield: 5.0 g; 1H NMR (500 MHz, CDCl3, ppm) δ 7.23-7.44 (m, 8H), 4.13 (q, 4H), 1.19 (t, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08633126B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-2b56f5493d7444798e5c727b7761c58b |
| Source note | uspto-grants-2014_01 |