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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410159Generated: October 27, 2026

Dimethyl Sulfide → HCID 136176942, compound

https://huagongshe.com/reaction/1410159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 86668982HCID 86668982—
SolventDiethyl EtherHCID 3283—
ProductHCID 136176942HCID 13617694271%

Reaction Steps

To a solution of 4-(3,5-dimethylisoxazol-4-yl)-3-(4-methoxyphenyl)-1-methyl-1H-pyrazole-5-carbaldehyde (4.1 mg, 0.013 mmol) in diethyl ether (3 mL) was added LiBH4 (12 mg, 0.55 mmol) and stirred at room temperature over night. The reaction was then quenched with water and extracted with EtOAc, filtered through a phase separator and concentrated. To the raw product in DCM (1 mL) was added BF3.Me2S (1 M solution in DCM, 0.2 mL, 0.2 mmol) and stirred over night at room temperature. The formed precipitate was twice washed with 0.5 mL DCM, dissolved in MeOH and purified on preparative HPLC to give E11 4-(4-(3,5-dimethylisoxazol-4-yl)-5-(hydroxymethyl)-1-methyl-1H-pyrazol-3-yl)phenol (2.8 mg, 0.009 mmol, 71%). ES/MS m/z: 299.6 (M+H), 297.7 (M−H); 1H NMR (MeOD, 500 MHz): 7.18 (m, 2H), 6.71 (m, 2H), 3.98 (s, 3H), 3.74 (s, 2H), 2.20 (s, 3H) and 1.87 (s, 3II).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921402B2
Source datasetuspto-grants-2014_12
ORD IDord-c800c1a66a274b3a9b0335c69ec12e32
Source noteuspto-grants-2014_12