HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553403Generated: October 26, 2026
Methanol → 3-(2-Nitrobenzylamino)-1-phenylpropanol
https://huagongshe.com/reaction/553403
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | 3-hydroxy-N-(2-nitrobenzyl)-3-phenyl propionic acid amide | HCID 67461894 | — |
| Reactant | HCID 178419153 | HCID 178419153 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(2-Nitrobenzylamino)-1-phenylpropanol | HCID 67461475 | — |
Reaction Steps
3-Hydroxy-N-(2-nitrobenzyl)-3-phenyl propionic acid amide (3.19 g, 10.6 mmol) was dissolved in tetrahydrofuran (50 ml) and under ice cooled condition, 1 M tetrahydrofuran-borane tetrahydrofuran solution (27.0 ml, 27.0 mmol) was added dropwise thereto. After the dropwise addition was finished, the reaction mixture was returned to room temperature and stirred for one hour, then heated to reflux for six hours and allowed to cool. Methanol (30 ml) was added thereto under ice cooled condition and heated to reflux for 30 minutes. After allowed to cool, the solvent was evaporated and 0.5 N hydrochloric acid water (30 ml) was added. After extracted with diethyl ether, the aqueous layer was adjusted to pH 8 with a saturated sodium hydrogen carbonate aqueous solution and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure to obtain 3-(2-nitrobenzylamino)-1-phenylpropanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08048825B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-7cf58015a401428da346147e801bd328 |
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| Source note | uspto-grants-2011_11 |
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