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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355204Generated: November 1, 2026

HCID 58869132, compound → HCID 58869160, compound

https://huagongshe.com/reaction/2355204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58869132HCID 58869132—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58869160HCID 5886916096%

Reaction Steps

To a solution of (7-benzenesulfonyl-4-oxo-chroman-2-ylmethyl)-methyl-carbamic acid tert-butyl ester (216 mg, 0.5 mmol) in THF (25 mL) at 0° C. was added MeMgCl (3.0 M in THF, 0.208 mL). The mixture was allowed to warm at room temperature and was stirred for 6 hours. The reaction was quenched by addition of water and it was concentrated in vacuo. The aqueous residue was extracted with DCM and the organic extracts were dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified via flash chromatography (DCM/MeOH, 97/3) to give (7-benzenesulfonyl-4-hydroxy-4-methyl-chroman-2-ylmethyl)-methyl-carbamic acid tert-butyl ester (214 mg, 96% yield) as yellow crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754759B2
Source datasetuspto-grants-2010_07
ORD IDord-f1e55cf9bf784cbdb5080aacd8cbc7c6
Source noteuspto-grants-2010_07