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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625544Generated: October 30, 2026

(S)-(-)-4-(4-hydroxybenzyl)-2-oxazolidinone → HCID 67422728, compound

https://huagongshe.com/reaction/1625544

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-(-)-4-(4-hydroxybenzyl)-2-oxazolidinoneHCID 11769373—
ReactantHCID 86632946HCID 86632946—
ProductHCID 67422728HCID 6742272877%

Reaction Steps

Compound 5a is synthesized by general procedure H from (S)-(−)-4-(4-hydroxybenzyl)-2-oxazolidinone (Tetrahedron; EN; 57; 39; 2001; 8313-8322) and 2-bromo-ethyl-methoxy-methyl-ether (Aldrich) at 10-fold scale in 77% yield (15.4 mmol, 4.33 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08784775B2
Source datasetuspto-grants-2014_07
ORD IDord-2cc6c49ffff240199b61c65e9944b1b9
Source noteuspto-grants-2014_07