HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899564Generated: October 30, 2026
N-Isopropyl-3-(2-hydroxy-5-methylphenyl)-3-phenylpropylamine → 2-(3-{[3-(2-BENZYLOXY-5-METHYLPHENYL)-3-PHENYLPROPYL]ISOPROPYLAMINO}-1-PHENYLPROPYL)-4-METHYLPHENOL
https://huagongshe.com/reaction/899564
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Isopropyl-3-(2-hydroxy-5-methylphenyl)-3-phenylpropylamine | HCID 9857017 | — |
| Reactant | HCID 86604788 | HCID 86604788 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(3-{[3-(2-BENZYLOXY-5-METHYLPHENYL)-3-PHENYLPROPYL]ISOPROPYLAMINO}-1-PHENYLPROPYL)-4-METHYLPHENOL | HCID 11563377 | — |
Reaction Steps
A mixture of N-isopropyl-3-(2-hydroxy-5-methylphenyl)-3-phenylpropylamine (59 g) and 3-(2-(benzyloxy)-5-methylphenyl)-3-phenylpropyl-4-methylbenzenesulfonate of Formula IVa (100 g) in acetonitrile (595 ml) was heated in an autoclave at 110-115° C. for 16-18 hours. The reaction mass was cooled to 60-65° C., and solvent was distilled completely under vacuum. Charged ethyl acetate (290 ml) and water (590 ml) to the residue. Separated the aqueous layer and extracted with 118 ml of ethyl acetate. Combined organic layers were washed with water (590 ml) and distilled completely to obtain 108 g of syrup. This syrup was loaded onto a silica gel column and eluted with 5% ethyl acetate in chloroform. Distilled the solvent completely to get 38 g of the title compound as syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07355077B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-1bec8830371c4d3db6a0faba9acdf4bb |
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| Source note | uspto-grants-2008_04 |
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