HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85307Generated: October 28, 2026
Lithium Bromide → 2-[(3-Methoxyphenyl)methylamino]ethanol
https://huagongshe.com/reaction/85307
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-((3-Methoxyphenyl)methyl)glycine ethyl ester | HCID 12867068 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[(3-Methoxyphenyl)methylamino]ethanol | HCID 4717257 | 135% |
Reaction Steps
Next, NaBH4 (3.8 g, 100 mmol) and LiBr (8.7 g, 100 mmol) were added to THF (100 ml), and the mixture was stirred at 80° C. for 1 hour. To this mixture, [(3-methoxyphenyl)methylamino]acetic acid ethyl ester (7.4 g, 33.1 mmol) dissolved in THF (20 ml) was added dropwise at room temperature. The mixture was stirred at 80° C. for 5 hours and further at room temperature for 16 hours. After the reaction solvent was evaporated to about half, KH2PO4 (1 M, 200 ml) was slowly added dropwise thereto. The organic layer was extracted with dichloromethane (50 ml) times and dried over Na2SO4 to give crude 2-[(3-methoxyphenyl)methylamino]ethanol (yield: 8.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846955B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-2e70cc22a940422ab8e1a922df0930ea |
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| Source note | uspto-grants-2014_09 |
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