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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530520Generated: November 1, 2026

Triethylamine → HCID 73291824, compound

https://huagongshe.com/reaction/530520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 86699945HCID 86699945—
SolventDichloromethaneHCID 6344—
ProductHCID 73291824HCID 7329182460%

Reaction Conditions

Temperature0 °C

Reaction Steps

Under nitrogen atmosphere at 0° C., to a stirred mixture of (2R,3S)-3-hydroxy-2-(2-phenethyloxyethoxy-carbonylamino)-butanoic acid (0.46 g, 1.18 mmol) in dry CH2Cl2 (35 mL), Et3N (0.49 mL, 3.55 mmol) and subsequently TBTU (0.30 g, 1.42 mmol) were added. The mixture was left stirring 1 h at 0° C. and 15 h at rt. Upon full conversion of the starting material, the organics were removed under reduced pressure, and the resulting crude product absorbed over silica gel and purified by typical column chromatography, eluting with Cy:EtOAc (from 100:0 to 0:100) to afford the pure title compound (0.18 g, 60%) as white solid. MS (ESI) m/z: 294 [M−H]+; (ESI) m/z: 292 [M−H]−. 1H NMR (DMSO-d6): δ 1.35 (d, J=6.4 Hz, 3H), 2.81 (t, J=7.1 Hz, 2H), 3.59 (t, 1H), 3.62 (t, J=6.3 Hz, 1H), 4.05-4.21 (m, 2H), 4.85 (dq, J=6.3 Hz, 1H), 5.43 (dd, J=6.1, 9.4 Hz, 1H), 7.15-7.33 (m, 5H), 8.33 (d, J=9.4 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353075B2
Source datasetuspto-grants-2016_05
ORD IDord-c8e635d877af473da4e5e52c7c98e730
Source noteuspto-grants-2016_05