HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986099Generated: October 27, 2026
Sodium hydride → Benzyloxyphenyl 6-methyloctyl ether
https://huagongshe.com/reaction/986099
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Bromo-6-methyloctane | HCID 13548105 | — |
| Reactant | 2-[2-[[2-(2,5-Dihydroxyphenyl)phenyl]methoxymethyl]phenyl]benzene-1,4-diol | HCID 131711022 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzyloxyphenyl 6-methyloctyl ether | HCID 20159468 | — |
Reaction Steps
A 100-ml 4-neck flask was charged with 3.74 g of NaH (containing 50% of oil) and 50 ml of N,N-dimethylformamide, and a solution of 15.46 g of hydroquinone monobenzyl ether in 30 ml of N,N-dimethylformamide was added under a nitrogen current over a period of 20 minutes in an ice water bath. After 20 minutes, 16 g of optically active 1-bromo-6-methyloctane was added over a period of 45 minutes, and reaction was carried out at room temperature for 6 hours. The reaction mixture was extracted with ether. The ether layer was washed with water, 5% NaOH, water and a saturated aqueous solution of sodium chloride in sequence and dried, and the organic solvent was distilled under reduced pressure to obtain a crude product. The crude product was purified to obtain 24.37 g of an ether compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04710585 |
|---|
| Source dataset | uspto-grants-1987_12 |
|---|
| ORD ID | ord-7561455b8ad04bf7a51d574c79016740 |
|---|
| Source note | uspto-grants-1987_12 |
|---|