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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398000Generated: October 30, 2026

Diisopropylethylamine → HCID 23001289, compound

https://huagongshe.com/reaction/398000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanesulfonic anhydrideHCID 81560—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 23001281HCID 23001281—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 23001289HCID 23001289—

Reaction Steps

To a solution of alcohol from Step H (2.99 g, 8.92 mmol) and N,N-diisopropylethylamine (4.66 mL, 26.8 mmol) in methylene chloride (100 mL)/ DMF (10 mL) was added di-tert-butyl dicarbonate (2.34 g, 10.7 mmol) at 0° C. The reaction was stirred for 24 hours, then methanesulfonic anhydride (3.11 g, 17.8 mmol) was added in one portion. The reaction was stirred for 3 hours at 25° C. and 16 hours at reflux. The reaction was poured onto saturated aqueous sodium bicarbonate and extracted with methylene chloride (3×100 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo to provide a yellow oil. The crude product was purified by column chromatography (30→80% ethyl acetate/hexane) to provide the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610722B2
Source datasetuspto-grants-2003_08
ORD IDord-56e5ccb7c677464ca404dcd09296ca7a
Source noteuspto-grants-2003_08