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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365496Generated: October 31, 2026

Trityl chloride → HCID 23292291, compound

https://huagongshe.com/reaction/365496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
ReactantHCID 178420883HCID 178420883—
SolventBenzeneHCID 241—
ProductHCID 23292291HCID 23292291—

Reaction Conditions

Temperature20 °C

Reaction Steps

1.25 ml (9 mmol) of triethylamine and 2.36 g (8.50 mmol) of trityl chloride are added, in succession, at 20° C., to a solution of the compound obtained in Example 16 (Step 4) in the form of the free amine (1.80 g, 8.40 mmol) in 50 ml of benzene, under nitrogen. After stirring for 15 hours at 20° C., the mixture is washed with H2O, and the organic phase is dried and concentrated in vacuo to yield an oily residue. Chromatography on a chiral column, eluting with a solution of triethylamine in toluene (0.5%), allows the 4 isomers to be separated in the form of white solids.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127396
Source datasetuspto-grants-2000_10
ORD IDord-b75a4999e9ba433eab964cc510f705e8
Source noteuspto-grants-2000_10