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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923817Generated: November 2, 2026

Dichloromethane → HCID 118625621, compound

https://huagongshe.com/reaction/923817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantOxt-101HCID 76444—
ReactantHCID 54595652HCID 54595652—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthyl AcetateHCID 8857—
SolventHeptaneHCID 8900—
ProductHCID 118625621HCID 118625621107.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

In step (c -2), 3′,4′,5′-trifluoro-[1,1′-biphenyl]-4-carboxylic acid (10.0 g, 37.0 mmol), 3-ethyl-3-hydroxymethyloxetane (5.9 g, 37 mmol), 4-dimethylaminopyridine (4.5 g, 37 mmol), and 100 ml of dichloromethane were mixed under nitrogen atmosphere and cooled to 0° C., and then 50 ml of a dichloromethane solution including 8.0 g (39 mmol) of dicyclohexylcarbodiimide was added dropwise thereto at 0° C., and the resulting mixture was stirred at room temperature for 15 hours. The mixture was filtrated by celite to collect a filtrate. The filtrate was condensed under a reduced pressure, followed by column chromatography (volume ratio of ethyl acetate:heptane=1:4) to obtain 13.9 g of (3-ethyloxetane-3-yl)methyl 3′,4′,5′-trifluoro-[1,1′-biphenyl]-4-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09279083B2
Source datasetuspto-grants-2016_03
ORD IDord-68b8dea0e28a491eb0e237ad6b42e9e7
Source noteuspto-grants-2016_03