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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369308Generated: October 30, 2026

Triethylamine → HCID 70872895, compound

https://huagongshe.com/reaction/2369308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactantbeta-D-Glucose pentaacetateHCID 2724702—
ReactantHCID 86672633HCID 86672633—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 70872895HCID 70872895—

Reaction Steps

2.11 g (5.41 mmol) of β-D-glucose pentaacetate and 1.0 g (4.2 mmol) of 4,8,12-trimethyltridec-3-en-1-ol were dissolved in dry acetonitrile (4 mL). 1.0 mL (8.3 mmol) of boron trifluoride diethyl etherate complex was added to the solution with cooling on ice. The reaction mixture was allowed to warm up slowly to room temperature while being stirred for 24 hours before addition of 1.7 mL (12 mmol) of triethylamine at 0° C. The resulting solution was diluted with ethyl acetate, and washed with water, 1M hydrochloric acid, saturated sodium bicarbonate aqueous solution, and saturated brine, successively, and dried over sodium sulfate. After filtration, the filtrate was concentrated to obtain 1-O-(4,8,12-trimethyltridec-3-enyl)-D-glucopyranoside tetraacetate as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703922B2
Source datasetuspto-grants-2014_04
ORD IDord-12477537d136458696dd1c41966524f4
Source noteuspto-grants-2014_04