HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416688Generated: October 29, 2026
Trimethyl borate → [3-(2-Aminoethyl)phenyl]methanol
https://huagongshe.com/reaction/416688
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | Methyl 3-(cyanomethyl)benzoate | HCID 10821136 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Lithium borohydride | HCID 4148881 | — |
| Product | [3-(2-Aminoethyl)phenyl]methanol | HCID 45091753 | 67% |
Reaction Steps
To a solution of methyl-3-(cyanomethyl)benzoate (4 grams, 0.023 mol, 1 molequivalent) in 5 ml dry THF, 2M LiBH4 in THF (60 ml, 5 molequivalents) and (MeO)3B (3 ml, 1 molequivalent) were added under nitrogen atmosphere. The reaction mixture was stirred and heated at 70-75° C. for 16-18 hours. After cooling, THF was evaporated, and 2NH2SO4 was added to the residue (to acidify the solution to pH of 1-2). The resulting solution was washed with ether and powdered K2CO3 was added to the aqueous phase until the pH reached 7. NaCl was then added and the solution was extracted with THF. The organic phase was dried over MgSO4 and the solvent was evaporated, to give a 2.3 grams (67%) of a pure product, which was used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088941B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-b79dc2eed556461aa335a347ac0aeef2 |
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| Source note | uspto-grants-2012_01 |
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