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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355228Generated: November 1, 2026

(R)-N-(7-benzenesulfonyl-chroman-2-ylmethyl)-2-benzyloxy-acetamide → (R)-N-(7-Benzenesulfonyl-chroman-2-ylmethyl)-2-hydroxy-acetamide

https://huagongshe.com/reaction/2355228

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-N-(7-benzenesulfonyl-chroman-2-ylmethyl)-2-benzyloxy-acetamideHCID 58869170—
ReactantHCID 178418361HCID 178418361—
SolventMethanolHCID 887—
Product(R)-N-(7-Benzenesulfonyl-chroman-2-ylmethyl)-2-hydroxy-acetamideHCID 1622576323,518.9%

Reaction Steps

(R)—N-(7-Benzenesulfonyl-chroman-2-ylmethyl)-2-benzyloxy-acetamide (100 mg, 0.22 mmol) and Perlman's catalyst (12 mg) were added to 15 mL MeOH and hydrogenated for 18 hours at 1.5 atmospheres of hydrogen. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure. The residue was purified by flash chromatography to give 18.7 g of (R)—N-(7-Benzenesulfonyl-chroman-2-ylmethyl)-2-hydroxy-acetamide, MS (M+H)=362.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754759B2
Source datasetuspto-grants-2010_07
ORD IDord-f305fc8ed78346a9aef351fe875f5d3f
Source noteuspto-grants-2010_07