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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625693Generated: October 29, 2026

3-(Methylthio)-1-propanol → HCID 118093707, compound

https://huagongshe.com/reaction/625693

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Methylthio)-1-propanolHCID 10448—
ReactantTriphenylphosphineHCID 11776—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
ReactantPotassium hydroxy sulfiteHCID 23707502—
ReactantHCID 118093744HCID 118093744—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 118093707HCID 118093707—

Reaction Steps

(1S,2S)-2-{4-[(R)-7-Fluoro-4-(3-fluoro-4-hydroxy-phenoxy)-indan-1-yloxy]-phenyl}-cyclopropanecarboxylic acid ethyl ester (Intermediate 9, 200 mg, 0.43 mmol), 3-methylthiopropanol (0.044 mL, 0.43 mmol), triphenylphosphine (120 mg, 0.47 mmol) and di-tert-butyl azodicarboxylate (110 mg, 0.47 mmol) are suspended in dry tetrahydrofuran (5 mL) and stirred overnight. A further quantity of 3-methylthiopropanol (0.044 mL, 0.43 mmol), and di-tert-butyl azodicarboxylate (110 mg, 0.47 mmol) are added and the mixture stirred for a further 24 hours. The solvent is removed under vacuum and the residue is purified by flash chromatography (gradient of ethyl acetate in cyclohexane) to give a residue which is suspended in a 1:1 mixture of tetrahydrofuran and water (4 mL) and oxone is added (380 mg, 0.62 mmol). The mixture is stirred for 2 hours then diluted with ethyl acetate and washed with water. The solvent is removed and the residue is purified by flash chromatography (0-50% ethyl acetate in cyclohexane) to give the title compound. (Yield 50 mg). LC (METHOD 5): tR=1.47 min; Mass spectrum (ES+): m/z=587 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09308194B2
Source datasetuspto-grants-2016_04
ORD IDord-7dab52df7df04ece97be3d39f3d04ce7
Source noteuspto-grants-2016_04