HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488945Generated: October 30, 2026
4-Chlorobenzyl alcohol → HCID 54305668, compound
https://huagongshe.com/reaction/1488945
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorobenzyl alcohol | HCID 13397 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 53730792 | HCID 53730792 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54305668 | HCID 54305668 | — |
Reaction Steps
0.3 g (10 mmol) of sodium hydride (80%) are stirred in 15 ml of tetrahydrofuran and 1.42 g (10 mmol) of 4-chlorobenzyl alcohol in 10 ml of tetrahydrofuran are added dropwise. The resulting clear solution is evaporated to dryness and a solution of 2.02 g (6.5 mmol) of 3-chloro-3-(3,4-dimethoxyphenyl)-1-morpholin-4-ylprop-2-en-1-one in 25 ml of dimethylformamide is added. The mixture is stirred at 90° C. for 20 hours. The solvent is then evaporated and the residue shaken with toluene/water. The organic phase is separated, washed with water, dried and purified over a flash column with 40 g of silicagel. Elution is carried out with toluene containing 10, 20 and 30% of acetone. The fractions with the TLC Rf-values 0.45 and 0.31 (toluene/acetone 7:3) are collected and evaporated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05677303 |
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| Source dataset | uspto-grants-1997_10 |
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| ORD ID | ord-e1463cda10a34129b429fa2219051f09 |
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| Source note | uspto-grants-1997_10 |
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