HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 53482763, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 53482708 | HCID 53482708 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 53482763 | HCID 53482763 | 52% |
Reaction Steps
Potassium tert-butoxide (32 mg, 0.28 mmol) was added to 4 (100 mg, 0.14 mmol) and tert-butyl-2-bromo acetate (105 mg, 0.54 mmol) in dry THF (3 ml). The reaction mixture was shaken for 30 min. Diethyl ether (10 ml and brine (5 ml) were added and the aqueous phase was extracted with ethyl acetate (3×20 ml). The combined organic phases were washed with brine and then dried with sodium sulfate. The volatile material was removed at reduced pressure and the crude product was purified by column chromatography (ethyl acetate/methanol 9:1), which gave 60 mg (52%) of 5. 1H-NMR (CDCl3); 3.91 (s, 2H), 3.66-3.52 (m, 48H), 3.51 (s, 2H), 3.45 (s, 6H), 3.37 (s, 9H), 1.46 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040637B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-1ab700dbf98b4cb6b0e185afcf4e0dff |
| Source note | uspto-grants-2015_05 |