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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2282886Generated: October 31, 2026

Sodium Hydroxide → HCID 52271559, compound

https://huagongshe.com/reaction/2282886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl (R)-1-Boc-3-fluoropyrrolidine-3-carboxylateHCID 86685754—
SolventMethanolHCID 887—
ProductHCID 52271559HCID 52271559—

Reaction Steps

To a solution of #166 (272 mg, 1.10 mmol, 1 eq.) dissolved in methanol (2.96 mL) was added an aqueous solution of sodium hydroxide (2.5 M, 0.88 mL) and the reaction was stirred at room temperature for 3.5 hours. The reaction was quenched with 10% aqueous citric acid (5 mL), ethyl acetate (100 mL) was added, and the layers separated. The organic layer was washed with 10% citric acid, water, and brine, dried over sodium sulfate, filtered and concentrated in vacuo to afford #168 as a white solid. (253 mg, 99%). 1H NMR (400 MHz, CDCl3), δ 3.96-3.69 (m, 3H), 3.59 (m, 1H), 2.59-2.33 (m, 2H), 1.51 (s, 9H). LC-MS (Protocol Q1): m/z 232.1 [M−H+], retention time=0.67 minutes. Chiral HPLC retention time: 3.39 min (purity=99%). (Column: Chiralpak AD-H, 4.6 mm×25 cm, mobile phase 5-60% CO2/Methanol, flow rate 3.0 mL/min); Optical rotation: [α]D25 4.8 (c=0.52, MeOH)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09138486B2
Source datasetuspto-grants-2015_09
ORD IDord-a5afa24983b142b5adebc1e028b93230
Source noteuspto-grants-2015_09