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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466805Generated: October 30, 2026

Ethanolamine → HCID 12494252, compound

https://huagongshe.com/reaction/466805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantDiethyl EtherHCID 3283—
ReactantPivalaldehydeHCID 12417—
ReactantHCID 10198312HCID 10198312—
SolventMethanolHCID 887—
SolventPentaneHCID 8003—
ProductHCID 12494252HCID 1249425293%

Reaction Steps

Dissolve B-(2-(trimethylsilyl)ethynyl)-9-borabicyclo[3.3.1]nonane.tetrahydrofuran complex (2.13 g, 7.3 mmol) in pentane (25 mL) and add trimethylacetaldehyde (795 μL, 7.3 mmol). Stir at room temperature for 5 days. Remove the solvent under a positive nitrogen pressure to give a yellow solid. Add ethyl ether (30 mL) and methanol (500 μL). Cool to 0° C. and add, by dropwise addition, ethanolamine (440 μL, 7.3 mmol). Stir overnight, centrifuge the reaction mixture and separate the clear supernatant liquid. Wash the precipitate with pentane (2×10 mL) and combine the organic phases. Wash with water (2×25 mL) and dry (MgSO4). Evaporate the solvent in vacuo and purify by silica gel chromatography (19:1 hexane/ethyl acetate) to give the title compound as a clear liquid (1.25 g, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05157167
Source datasetuspto-grants-1992_10
ORD IDord-d2408bb7c5294521a2931844d78cf054
Source noteuspto-grants-1992_10