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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132656Generated: November 1, 2026

Triethylamine → HCID 11240761, compound

https://huagongshe.com/reaction/132656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 86597964HCID 86597964—
SolventMethanolHCID 887—
ProductHCID 11240761HCID 1124076185.6%

Reaction Steps

(3R,4R,5R)-3-Amino-4,5-dimethyl-heptanoic acid hydrochloride (10.8 g, 51.5 mmol) was dissolved in 50 mL of methanol. To this solution was added triethylamine (5.2 g, 7.2 mL, 51.5 mmol). The solution was stirred for 10 minutes and then evaporated to a flocculent solid. Dichloromethane (376 mL) was added and the resulting slurry was stirred at room temperature for 45 minutes. Next, 188 mL of acetonitrile was added and the slurry was stirred for 30 minutes and then filtered. The solids were washed with 20 mL of 2:1 (v/v) dichloromethane-acetonitrile and dried on a nitrogen press to give 7.64 g (85.6% yield) of the titled compound as a white solid: 1H NMR (CD3OD, 399.77 MHz) 0.88 (t, J=7.5 Hz, 3H), 0.91 (d, J=7.0 Hz, 3H), 0.94 (d, J=6.6 Hz, 3H), 0.98-1.12 (m, 1H), 1.32-1.43 (m, 1H), 1.43-1.64 (m, 2H), 2.26 (dd, J=16.5, 9.9 Hz, 1H), 2.47 (dd, J=9.5, 3.7 Hz, 1H), 3.28-3.36 (m, 1H). Low resolution mass spec: nominal m/e calc'd for C9H19NO2 (M+H)+: 174. Found: m/e 174.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07388023B2
Source datasetuspto-grants-2008_06
ORD IDord-7dc9a0458aa3499bb0a8ede2355f9222
Source noteuspto-grants-2008_06