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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211329Generated: October 31, 2026

20039-37-6 → HCID 57097671, compound

https://huagongshe.com/reaction/2211329

Reaction equation

Participants

RoleNameHCIDCharge
Reactant20039-37-6HCID 18757208—
ReactantHCID 57313420HCID 57313420—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 57097671HCID 5709767164.5%

Reaction Steps

79.6 g (0.63M) of the optically active alcohol (V) obtained in 1-4) above was dissolved in 300 ml of methylene chloride and the resulting solution was added dropwise to a suspension of 304 g (0.81M) of pyridine dichromate in 700 ml of methylene chloride at room temperature. Then the resulting mixture was stirred for three days. The obtained reaction mixture was diluted with 1 l of diethyl ether and filtered through celite. The filtrate was dried over anhydrous magnesium sulfate and the solvent was evaporated. The residue was distilled under reduced pressure to give 50.4 g (theoretical yield: 64.5%) of the aimed compound (VI) as a colorless oily material. b.p.: 70° C./20 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05463118
Source datasetuspto-grants-1995_10
ORD IDord-08c384a4b6ec466aa3f88e5e2a55a50b
Source noteuspto-grants-1995_10