HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380741Generated: October 31, 2026
Benzyl Chloride → HCID 18365999, compound
https://huagongshe.com/reaction/380741
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 18366005 | HCID 18366005 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18365999 | HCID 18365999 | 85.2% |
Reaction Steps
2.5 g (11.0 mmol) of 3-(4-hydroxytetrahydrofuran-3-yloxy)-4-methoxybenzonitrile (A 15) in 12 ml of dimethylformamide are added dropwise under a nitrogen atmosphere to a solution of 350 mg (12.0 mmol) of sodium hydride in 12 ml of dimethylformamide and the mixture is heated at 40° C. for 1 h. 1.6 ml (13.0 mmol) of benzyl chloride, dissolved in 6 ml of dimethylformamide, are then added dropwise at RT. The mixture is stirred at RT for 4 h. concentrated, treated with 50 ml of water and acidified with 2 N hydrochloric acid. After extraction with 3×40 ml of ethyl acetate, the combined organic phases are washed with saturated sodium chloride solution, dried over magnesium sulfate and concentrated. For further purification, the product is chromatographed on silica gel [toluene/ethyl acetate=4:1]. The product-containing fractions are concentrated and the residue is crystallized from isopropanol. 3.05 g of the title compound of m.p. 72-75° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06303789B1 |
|---|
| Source dataset | uspto-grants-2001_10 |
|---|
| ORD ID | ord-db9970d6741a419ebe63784501f93038 |
|---|
| Source note | uspto-grants-2001_10 |
|---|