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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206967Generated: October 31, 2026

1-Butanol, 4-chloro-, 1-acetate → HCID 118324351, compound

https://huagongshe.com/reaction/2206967

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Butanol, 4-chloro-, 1-acetateHCID 23399—
ReactantSodium AzideHCID 33557—
SolventDimethylformamideHCID 6228—
ProductHCID 118324351HCID 11832435181%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a 500 mL flask was added 5.0 g (33 mmol, 1.0 eq) of 4-chlorobutylacetate and dissolved in 100 mL of DMF. Next 2.6 g (40 mmol, 1.2 eq) of sodium azide was added by a glass pipette. A water condenser was placed onto the flask and the reaction heated to 80° C. for 16 hr with stirring. The reaction was then cooled to room temperature and quenched with 300 mL of water to dissolve the sodium salts. The aqueous solution was extracted with diethyl ether 3×100 mL. The organic layers were combined and dried with MgSO4. The solution was filtered and concentrated under vacuum with no external heat, resulting in 4-azido-1-butylacetate (4.22), which was carried onto the next step without further purification; 1H NMR (CDCl3, 300 MHz): δ: 4.04 (t, J=6.0 Hz, 2H), 3.27 (t, J=6.2 Hz, 2H), 2.00 (s, 3H), 1.76-1.52 (m, 4H). 13C NMR (75 MHz, CDCl3) δ: 170.82, 63.55, 50.84, 25.73, 25.39, 20.73. 81% yield, clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376385B2
Source datasetuspto-grants-2016_06
ORD IDord-b5930feab76e47b994d4bd63c842336b
Source noteuspto-grants-2016_06