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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232122Generated: October 29, 2026

4-Toluenesulfonyl chloride → HCID 18633338, compound

https://huagongshe.com/reaction/232122

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
ReactantHCID 14649527HCID 14649527—
SolventDichloromethaneHCID 6344—
ProductHCID 18633338HCID 1863333893%

Reaction Steps

200 mg of the compound obtained in Example 10 was dissolved in 2 ml of dry methylene chloride, and 115 μl of triethylamine and 152 mg of tosyl chloride were added thereto. The mixture was stirred at room temperature overnight. Then, 115 μl of triethylamine was further added, and the mixture was reacted at room temperature and then evaporated to dryness under reduced pressure. A solution mixture of benzene/ethyl acetate (30/1) was added to the residue. After filtering insolubles off, the filtrate was purified by silica gel column chromatography to obtain 281 mg of (4S,5S)-3-tert-butyloxycarbonyl-2,2-dimethyl-5-(2-p-toluenesulfonyloxyethyl)-4-isobutyloxazolidine as a syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04851387
Source datasetuspto-grants-1989_07
ORD IDord-59d2dfbb57674887985a9207315dbd9a
Source noteuspto-grants-1989_07