HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982464Generated: October 26, 2026
Dichloromethane → 3-Methylthio4-n-propoxy-5-benzyloxybenzaldehyde
https://huagongshe.com/reaction/982464
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 1-Bromopropane | HCID 7840 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Methylthio-4-hydroxy-5-benzyloxybenzaldehyde | HCID 11778108 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Methylthio4-n-propoxy-5-benzyloxybenzaldehyde | HCID 10471022 | — |
Reaction Steps
64.5 g of 3-methylthio-4-hydroxy-5-benzyloxybenzaldehyde dissolved in a 75 mL of DMF was treated with 50 g of K2CO3 and 32 g of 1-bromopropane and stirred overnight at 70° C. The next day about 1.5 liters of methylene chloride and an equal amount of water was added to the reaction mixture. The organic layer was removed, washed three times with distilled water, dried over MgSO4 and evaporated to yield the title compound as viscous liquid that solidified slowly: NMR(200 MHz, CDCl3) δ 1.02 (t, CH2CH2CH3), 1.82 (m, CH2CH2CH3), 2.48 (s, SCH3), 4.12 (t, OCH2CH2CH3), 5.18 (s, OCH2Ar), 7.26-7.52 (m, ArH), 9.86 (s, ArCHO).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04996203 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-7c6f617027084c2da8ae4a9564192c34 |
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| Source note | uspto-grants-1991_02 |
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