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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493111Generated: November 1, 2026

4-Toluenesulfonyl chloride → HCID 53951603, compound

https://huagongshe.com/reaction/1493111

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantHCID 53826896HCID 53826896—
SolventPyridineHCID 1049—
ProductHCID 53951603HCID 5395160361.6%

Reaction Steps

To an ice-cool solution of the diol prepared according to g) (2.0 g, 10.2 mmole) in pyridine (22 ml) was added p-toluenesulfonyl chloride (2.13 g, 11.2 mmole) in small portions and over 30 min. The mixture was stirred at 0° for 30 min and then stored overnight at 3°. The usual extraction with ether and treatment of the organic phase gave 2.85 g of a crude product which, on thin layer chromatographic analysis, showed two components. The further purification of this product by MPLC [LOBAR® column (origin: Merck), mixture of hexane-ethyl acetate as elution agent] gave 2.20 g (yield: 61.6%) of the desired product, i.e. 6-hydroxy-4,9-dimethyl-3,7,9-decatrienyl p-toluenesulfonate, and 220 mg of an unidentified by-product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05021402
Source datasetuspto-grants-1991_06
ORD IDord-8ff6a1f6601046a1bb12f4e82bc3da3e
Source noteuspto-grants-1991_06