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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257151Generated: October 29, 2026

Dichloromethane → HCID 19784616, compound

https://huagongshe.com/reaction/257151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantStearyl AlcoholHCID 8221—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantHCID 19784608HCID 19784608—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 19784616HCID 1978461669.3%

Reaction Steps

A solution of 3.24 g (10.0 mmol) of 2-(2-allyloxy-5-tert-butylphenyl)-2-phenylacetic acid (compound (105), Example 2) and 2.70 g (10.0 mmol) of stearyl alcohol (1-octadecanol) in 25 mol of dichloromethane is treated with 100 mg (0.82 mmol) of 4-dimethylaminopyridine and 2.20 g (10.7 mmol) of N,N'-dicyclohexylcarbodiimide, and the mixture is stirred for 60 hours at room temperature. The reaction mixture is filtered and concentrated on a vacuum rotary evaporator. Chromatography of the residue from silica gel using the diluent system dichloromethane/hexane=1:1 yields 4.0 g (69%) of stearyl 2-(2-allyloxy-5-tert-butylphenyl)-2-phenylacetate (compound (106), Table 1) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05260430
Source datasetuspto-grants-1993_11
ORD IDord-271d286a7ac74507a81a12a137bee09f
Source noteuspto-grants-1993_11