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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58358Generated: October 29, 2026

Methanol → (S)-2-[(S)-3-(4-Allyloxy-phenyl)-2-tert-butoxycarbonylamino-propionylamino]-4-methyl-pentanoic acid

https://huagongshe.com/reaction/58358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactant(S)-2-[(S)-3-(4-Allyloxy-phenyl)-2-tert-butoxycarbonylamino-propionylamino]-4-methyl-pentanoic acid methyl esterHCID 86650238—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(S)-2-[(S)-3-(4-Allyloxy-phenyl)-2-tert-butoxycarbonylamino-propionylamino]-4-methyl-pentanoic acidHCID 66847292—

Reaction Steps

Methyl ester 1 (8.45 g, 18.8 mmol) was dissolved in THF (35 mL) and sodium hydroxide (1.13 g, 28.2 mmol) pre-dissolved in water (10 mL) was added. A further 15 mL of THF and 20 mL of methanol were added to obtain a homogenous solution. The reaction mixture was stirred at rt for 18 h before being concentrated in vacuo. The residue was partitioned between EtOAc and 1M hydrochloric acid. The aqueous phase was extracted twice more with EtOAc and the combined organic extracts were washed with brine, dried (MgSO4), filtered and concentrated in vacuo to yield a white foam, 7.25 g, 89%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434762B2
Source datasetuspto-grants-2016_09
ORD IDord-c8b4f35a7d9541918528705f25394f39
Source noteuspto-grants-2016_09