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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
ReactantMethyl 3-(cyanomethyl)benzoateHCID 10821136—
SolventTetrahydrofuranHCID 8028—
SolventLithium borohydrideHCID 4148881—
Product[3-(2-Aminoethyl)phenyl]methanolHCID 4509175367%

Reaction Conditions

Temperature72.5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088941B2
Source datasetuspto-grants-2012_01
ORD IDord-b79dc2eed556461aa335a347ac0aeef2
Source noteuspto-grants-2012_01