HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739412Generated: November 3, 2026
4-Hydroxybenzaldehyde → HCID 21841070, compound
https://huagongshe.com/reaction/1739412
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Chloropropyl phenyl sulfide | HCID 269606 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21841070 | HCID 21841070 | 82.3% |
Reaction Steps
0.69 g of 4-hydroxybenzaldehyde were dissolved in 30 ml of DMF, and the resultant solution was further added with 0.24 g of 60% NaH while cooling the solution with ice and then stirred for 1 hour after elevating the temperature of the solution to room temperature. Further, the solution was fed dropwise with 1.0 g of 1-chloro-3-phenylthio propane while cooling the solution with ice and then stirred for 1 hour at room temperature and further for a night at 50-60° C. After completed the reaction, the solution reacted was poured into ice-water and extracted with ethyl acetate. The organic layer resulted was then washed with aqueous solution of sodium hydroxide and dried with anhydrous magnesium sulfate, and the solvent used was removed by distillation under reduced pressure, thereby affording 1.2 g of 4-(3-phenylthiopropyloxy)-benzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05965743 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-543005b2997143fd94378af7ac570ee1 |
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| Source note | uspto-grants-1999_10 |
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