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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247018Generated: November 1, 2026

Triethylamine → HCID 86604079, compound

https://huagongshe.com/reaction/1247018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium AzideHCID 33557—
ReactantMethanesulfonic anhydrideHCID 81560—
ReactantHCID 69587602HCID 69587602—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86604079HCID 8660407918.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a suspension of the product from Step D (0.90 g, 3.45 mmol) in tetrahydrofuran (20 mL) was added triethylamine (1.93 mL, 13.9 mmol); this mixture was cooled (ice bath), methane sulfonic anhydride (1.20 g, 6.92 mmol) was added, and the mixture was stirred for 20 minutes. Sodium azide (2.25 g, 34.6 mmol) was added and the mixture was evaporated to a residue which dissolved in dimethyl sulfoxide (20 mL) and heated at 90° C. for 2.5 hours. The reaction mixture was cooled to room temperature, water (200 mL) was added, and the mixture was extracted with ethyl acetate (2×100 mL). The combined extracts were washed with water (100 mL), dried (magnesium sulfate), filtered, and evaporated to solid (0.97 g). This residue was purified by chromatography (silica gel, ethyl acetate gradient) and recrystallized from methanol and ethyl acetate to give a colorless solid (0.18 g, 18%): mp 162–164° C.; LC/MS m/z 286.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129257B1
Source datasetuspto-grants-2006_10
ORD IDord-98ee36de372740f4a74afb5bf7424b81
Source noteuspto-grants-2006_10