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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043404Generated: October 30, 2026

2,4-Dichlorophenol → HCID 56649063, compound

https://huagongshe.com/reaction/1043404

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichlorophenolHCID 8449—
ReactantTriethylamineHCID 8471—
ReactantPhosphorodichloridic acid, phenyl esterHCID 13038—
Reactant39825-33-7HCID 13089460—
SolventDichloromethaneHCID 6344—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 56649063HCID 5664906366%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Phenyl phosphorodichloridate (10.0 g, 47.4 mmol) was dissolved in 60 mL of dry DCM and subsequently cooled to −78° C. Slow addition of a preformed mixture of 2,4-dichlorophenol (7.73 g, 47.4 mmol) and triethylamine (7.27 mL, 52.1 mmol) in 20 mL of DCM was followed by stirring at above temperature for 30 min. The reaction was brought to 0° C. and stirred for 2.5 h at this temperature before (L)-alanine isopropyl ester (7.95 g, 47.4 mmol) was added as a solid in one batch. Stirring for 40 min at 0° C. was then followed by addition of more triethylamine (13.9 mL, 99.54 mmol) and additional stirring for 3 h at 0° C. or until judged complete by TLC (ethyl acetate/hexane=1/3). The reaction mixture was subsequently evaporated under reduced pressure and finally submitted to column chromatography (ethyl acetate in hexane) on silica gel to yield the product (mixture of two isomers) in 66% yield (13.6 g) as a viscous colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563530B2
Source datasetuspto-grants-2013_10
ORD IDord-9d11396abde641069246eb982963eabb
Source noteuspto-grants-2013_10