HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357309Generated: October 25, 2026
4-(4-(2-Amino-2-methylpropyl)phenoxy)benzamide → (S)-4-(4-[2-(N-[3-(2-amino-3-nitrophenoxy)-2-hydroxypropyl]amino)-2-methylpropyl]phenoxy)benzamide
https://huagongshe.com/reaction/357309
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(4-(2-Amino-2-methylpropyl)phenoxy)benzamide | HCID 11832961 | — |
| Reactant | (S)-3-(2-Amino-3-nitrophenoxy)-1,2-epoxypropane | HCID 15049327 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (S)-4-(4-[2-(N-[3-(2-amino-3-nitrophenoxy)-2-hydroxypropyl]amino)-2-methylpropyl]phenoxy)benzamide | HCID 54045428 | 62% |
Reaction Steps
A suspension of (S)-3-(2-amino-3-nitrophenoxy)-1,2-epoxypropane (5 g, 23.8 mmol) and 4-(4-(2-amino-2-methylpropyl)phenoxy)benzamide (20.3 g 71.1 mmol) in absolute ethanol (200 mL) was heated to 55° C. for 12 h. All solids went into solution at 50° C. Upon completion of the reaction, the solvent was evaporated to dryness. The residue was redissolved in ethyl acetate and washed with a saturated solution of sodium bicarbonate. The layers were separated and the aqueous phase was extracted with ethyl acetate. The two organic layers were combined and washed with brine. The phases were separated and the organic layer was dried over sodium sulfate, filtered, and the solvent evaporated. column chromatography eluting with 20% MeOH/CHCl3 gave 7.26 g (62%) of product. NMR. MS.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05840738 |
|---|
| Source dataset | uspto-grants-1998_11 |
|---|
| ORD ID | ord-799b432b234448928455bc3574ac0dc9 |
|---|
| Source note | uspto-grants-1998_11 |
|---|