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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718005Generated: October 29, 2026

Acetic Acid → HCID 86713712, compound

https://huagongshe.com/reaction/718005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthanolamineHCID 700—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86713711HCID 86713711—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 86713712HCID 86713712—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of C6 (338 mg, 1.52 mmol) in methanol (5 mL) was added 2-aminoethanol (139 mg, 2.28 mmol) followed by acetic acid (89 μL, 1.55 mmol). The reaction was stirred at reflux for 2 hours, then cooled to 0° C. Sodium borohydride (115 mg, 3.04 mmol) was added and the mixture was allowed to warm to room temperature. The reaction was diluted with ethyl acetate, quenched with water, and then extracted three times with ethyl acetate. The combined organic layers were dried over sodium sulfate and concentrated in vacuo to provide the crude title compound as a liquid. Yield: 362 mg, 1.35 mmol, 89%. This was presumed to be a mixture of stereoisomers. LCMS m/z 268.3 (M+1). 1H NMR (400 MHz, CDCl3), characteristic peaks: δ 7.22-7.28 (m, 2H), 7.10-7.16 (m, 2H), 3.63 (dd, J=5.3, 5.1 Hz, 2H), 2.75 (dd, J=5.3, 5.1 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193726B2
Source datasetuspto-grants-2015_11
ORD IDord-105e2ca12c2c4946b79640dae2a77cbf
Source noteuspto-grants-2015_11