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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612814Generated: November 3, 2026

Diethylamine → HCID 131717794, compound

https://huagongshe.com/reaction/1612814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
ReactantHCID 53842677HCID 53842677—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131717794HCID 131717794—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 75 mg 90.35 mmole) of (2R-cis)-3-nonyloxiranecarboxylic acid and 0.148 ml (106 mg, 1.05 mmole) of triethylamine in 5 ml of THF was prepared under argon and cooled to 0° C. To this solution 50 mg (0.37 mmole) of isobutylchloroformate was added and the mixture was allowed to stir of 30 min. Diethylamine (0.109 ml, 76 mg, 1.05 mmole) was then added and the mixture stirred for an additional 2 hours. The reaction was diluted with 75 ml of Et2O, washed with 50 ml of saturated NaHCO3, 30 ml of brine, dried over MgSO4, filtered and evaporated to yield a clear residue. This residue was flash chromatographed (25 mm column; 5% MeOH:CHCl3) to afford 80 mg of a clear oil. 1H NMR 3.57 (d, 1, J=4 Hz), 3.6-3.3 (m, 4), 3.2 (m, 1), 1.6-1.2 (m, 19), 1.13 (t, 3, J=7 Hz), 0.88 (t, 3, J=7 Hz). Mass Spectra: M+(1.5)269, M-OH(1.3)252, M(100)100.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05190969
Source datasetuspto-grants-1993_03
ORD IDord-d25de8b3c76f4b3dbb0310c63534372c
Source noteuspto-grants-1993_03