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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522359Generated: October 29, 2026

Hydrochloric Acid → HCID 89590945, compound

https://huagongshe.com/reaction/522359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantDiisopropylethylamineHCID 81531—
ReactantTriphosgeneHCID 94429—
ReactantL-tert-LeucineHCID 164608—
ReactantHCID 58158109HCID 58158109—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 89590945HCID 89590945—

Reaction Conditions

Temperature22 °C

Reaction Steps

To a stirred solution of (1R,2S)-2-(but-3-en-1-yl)cyclopentanol (see International Patent Application Publication No. WO2009/134624) (2.1 g) and DIPEA (5.3 mL) in anhydrous 1,4-dioxane (51 ml), at 10° C. and under nitrogen, was added a solution of triphosgene (1.5 g) in dioxane (51 ml). This reaction was stirred at 22° C. for 1.5 hour and 3-methyl-L-valine (2 g) and NaOH (1M, 30.5 mL) were added, then stirred at 70° C. for 15 hours. At 22° C., the reaction solution was acidified to pH 3 with 1 N HCl and extracted with (3×100 ml) ether. The combined organic layer were washed with water (100 ml), brine (70 ml), dried over Na2SO4, filtered and concentrated. The residue was purified by flash chromatography (silica gel, eluting with 10 to 100% EtOAc in hexane) to give the desired product (3.26 g). LRMS (ES+) M/Z (M+Na)+ 320.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328138B2
Source datasetuspto-grants-2016_05
ORD IDord-55cae77396fb47c09a37a721fb4d2762
Source noteuspto-grants-2016_05