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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114289Generated: October 31, 2026

Acetic Acid → HCID 59773620, compound

https://huagongshe.com/reaction/2114289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDiisopropylamineHCID 7912—
Reactant2,4,6-Triisopropylbenzenesulfonyl azideHCID 371707—
ReactantHCID 59773514HCID 59773514—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59773620HCID 59773620—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2.5 eq of diisopropylamine in 50 mL of dry THF was cooled to −78° C. While stirring, 2.4 eq of n-BuLi (2.5 M in hexanes) was added dropwise. The reaction mixture was warmed to 0° C. After stirring for 30 min, the solution was cooled to −78° C. and 1.0 eq of 97 dissolved in 20 mL of dry THF was added. After stirring at −78° C. for 30 min, 1.5 eq of trisyl azide was added. The mixture was stirred, as it warmed to rt. After 17 hrs, 4.5 eq of 17 M glacial acetic acid was added and stirred at rt for 5 hrs. The reaction mixture was rotary evaporated and 30 mL of saturated NaHCO3 was added. The mixture was extracted with EtOAc (3×50 mL). The combined organic extracts were dried over MgSO4 and vacuum filtered. The filtrate was rotary evaporated and flash chromatographed on silica using EtOAc as eluent. After concentration and drying under vacuum of the fractions containing product, a brownish colored solid was obtained as 98.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432379B2
Source datasetuspto-grants-2008_10
ORD IDord-878d796720a74b5091473418c5a9df28
Source noteuspto-grants-2008_10