HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522359Generated: October 29, 2026
Hydrochloric Acid → HCID 89590945, compound
https://huagongshe.com/reaction/522359
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | L-tert-Leucine | HCID 164608 | — |
| Reactant | HCID 58158109 | HCID 58158109 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 89590945 | HCID 89590945 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328138B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-55cae77396fb47c09a37a721fb4d2762 |
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| Source note | uspto-grants-2016_05 |
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