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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167915Generated: November 1, 2026

Hydrochloric Acid → (3S,5R)-5-Methyl-3-(toluene-4-sulfonyloxymethyl)-octanoic Acid Tert-butyl Ester

https://huagongshe.com/reaction/1167915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant(3S,5R)-3-Hydroxymethyl-5-methyl-octanoic Acid Tert-butyl EsterHCID 57070108—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(3S,5R)-5-Methyl-3-(toluene-4-sulfonyloxymethyl)-octanoic Acid Tert-butyl EsterHCID 5717850091.1%

Reaction Steps

To alcohol 103 (1.98 g, 8.1 mmol) in CH2Cl2 (40 mL) at room temperature was added triethylamine (2.4 g, 0.024 mol), DMAP (20 mg) and tosyl chloride (2.3 g, 0.012 mol). After 14 hours 1N HCl was added and the two layers separated. The aqueous phase was extracted with ether and the combined organic phases dried (MgSO4) and concentrated. Flash chromatography (95% hexane/EtOAc) gave tosylate 104 as an oil (2.94 g, 91%). 13C NMR (100 MHz; CDCl3) 171.60, 144.92, 133.07, 130.02, 128.12, 80.80, 72.15, 39.73, 38.09, 37.89, 32.67, 29.71, 28.22, 21.83, 20.10, 19.54, 14.49.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620829B2
Source datasetuspto-grants-2003_09
ORD IDord-b26f7db541ec4af9a743d2af245fc741
Source noteuspto-grants-2003_09