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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746417Generated: October 31, 2026

Diethyl Ether → HCID 71543440, compound

https://huagongshe.com/reaction/1746417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 86731592HCID 86731592—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 71543440HCID 71543440—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of ethyl 4-(4-((3,5-dimethylisoxazol-4-yl)methoxy)-N-isobutylphenylsulfonamido)-3-methylbenzoate (40 mg, 0.080 mmol) in THF (5 mL) stirred under nitrogen at 0° C. was added a solution of LiAlH4 1M in diethyl ether (0.160 mL, 0.160 mmol) dropwise. The reaction mixture was stirred at 0° C. for 30 minutes. The reaction was then allowed to warm up to room temperature and stirred for 2 hours. The reaction mixture was diluted with dichloromethane (10 mL). The organic phase was washed with water 10 mL, and saturated brine 10 mL, dried using a hydrophobic frit and concentrated under a stream of nitrogen in the Radleys blowdown apparatus to give the crude product. The crude was dissolved in 1:1 MeOH:DMSO 1 mL and purified by mass directed autoprep on a Sunfire C18 column using acetonitrile:water with a formic acid modifier. The solvent was dried under a stream of nitrogen in the Radleys blowdown apparatus to give the required product, 23.6 mg colorless oil which solidified. LCMS (M+1) 459, RT 1.14 mins.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150508B2
Source datasetuspto-grants-2015_10
ORD IDord-3f23f0ca9a0f4738a5d2800b22028bb1
Source noteuspto-grants-2015_10