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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808785Generated: November 2, 2026

Sodium Hydroxide → HCID 57543943, compound

https://huagongshe.com/reaction/1808785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium SulfateHCID 24436—
ReactantHCID 14804461HCID 14804461—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57543943HCID 57543943—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of tert-butyl 2-methyl-1-oxo-1-(pyrrolidin-1-yl)propan-2-ylcarbamate (Compound F5) (2.696 g, 10.52 mmol) in THF (20 mL) was a 1M LAH in THF (42.1 mL, 42.07 mmol) solution dropwise added (over approximately 10 min) at 0° C. under a nitrogen atmosphere. The resultant mixture was stirred at rt for 1 h and heated at 40° C. over night. The reaction was cooled to 0° C. and Na2SO4×10H2O followed by NaOH (2M, 2 mL) was added. The mixture was diluted with Et2O (100 mL) and the resultant mixture was filtered. The solids were washed with Et2O (3×50 mL). To the filtrate was HCl (1.25 N aq. solution, 15 mL) in EtOH added. The filtrate was concentrated and the residue mixed with EtOH (60 mL). The EtOH was removed under reduced pressure. IPA (30 mL) was added and the mixture sonicated for 2 min. After filtration was the title compound (1.89 g, 96%) obtained as a HCl salt. 1H NMR (400 MHz, CDCl3) δ 1.00, 1.71, 2.29, 2.41, 2.63. Total no of protons: 19.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08361998B2
Source datasetuspto-grants-2013_01
ORD IDord-2f86a40231b24ec589a3789983328152
Source noteuspto-grants-2013_01