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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174388Generated: October 30, 2026

Lithium Hydroxide → HCID 86707798, compound

https://huagongshe.com/reaction/2174388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
ReactantHCID 86707797HCID 86707797—
SolventMethanol tetrahydrofuran waterHCID 21892291—
ProductHCID 86707798HCID 8670779874%

Reaction Steps

To a stirred suspension of 1-{2-Chloro-4-[5-(3,4,5-trichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-phenyl}-azetidine-3-carboxylic acid methyl ester (Preparation 13, 0.55 g, 1.086 mmol) in THF:MeOH:H2O (1:1:1, 9 mL) was added lithium hydroxide (0.228 g, 5.43 mmol) at room temperature. Resulting reaction mixture was stirred at room temperature for 18 hours. After consumption of starting material, reaction mixture was concentrated in vacuo; acidified with 1N HCl up to pH ˜5. Acidified aqueous layer was extracted with ethyl acetate (5×20 mL). Combined organic layer was dried over sodium sulphate and evaporated under reduced pressure and was triturated with n-pentane (25 mL) to afford off white solid (0.4 g, 74%). 1H NMR (400 MHz, DMSO-d6) δ: 3.45-3.50 (m, 1H), 4.12-4.16 (m, 2H), 4.26-4.33 (m, 4H), 6.67 (d, 1H, J=9.04 Hz), 7.51-7.53 (m, 2H), 7.81 (s, 2H), 12.75 (bs, 1H); LC-MS (M+H): =528.80.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09061013B2
Source datasetuspto-grants-2015_06
ORD IDord-3eefa9196b3c41b583c449e9538bd7b2
Source noteuspto-grants-2015_06