Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371322Generated: October 25, 2026

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

https://huagongshe.com/reaction/2371322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactant(S)-2-[(S)-3-(4-Allyloxy-phenyl)-2-tert-butoxycarbonylamino-propionylamino]-3-methyl-butyric acid methyl esterHCID 14632374—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(S)-2-[(S)-3-(4-Allyloxy-phenyl)-2-tert-butoxycarbonylamino-propionylamino]-3-methyl-butyric acidHCID 66847200—

Reaction Steps

Methyl ester 42 (4.90 g, 11.3 mmol) was dissolved in THF (35 mL) and sodium hydroxide (17 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, 4.60 g, 97%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710178B2
Source datasetuspto-grants-2014_04
ORD IDord-fc416837675b42e1b3eb90f93f559abf
Source noteuspto-grants-2014_04