HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → 1-Phenyl-2,5,8,11-tetraoxatridecan-13-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Tetraethylene Glycol | HCID 8200 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Sodium Chloride | HCID 5234 | — |
| Product | 1-Phenyl-2,5,8,11-tetraoxatridecan-13-ol | HCID 11076957 | 71% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To the oil of non-polydispersed tetraethylene glycol (19.4 g, 0.10 mol) was added a solution of NaOH (4.0 g in 4.0 mL) and the reaction was stirred for 15 mm. Then benzyl chloride (3.54 mL, 30.8 mmol) was added and the reaction mixture was heated to 100° C. and stirred overnight. The reaction mixture was cooled to room temperature, diluted with sat. NaCl (250 mL), and washed CH2Cl2 (2×200 mL). The organic layers were combined, washed sat. NaCl, dried MgSO4, and chromatographed (silica, ethyl acetate) to afford the non-polydispersed title compound as a yellow oil (6.21 g, 71% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08030269B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-de57bb28a1dc402788c16ee75cbc1aed |
| Source note | uspto-grants-2011_10 |