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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014983Generated: October 30, 2026

Dicyclohexylcarbodiimide → HCID 86761365, compound

https://huagongshe.com/reaction/1014983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant3-PentanolHCID 11428—
ReactantHCID 86761364HCID 86761364—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 86761365HCID 8676136537%

Reaction Steps

[{1α,3β-Bis(tert-butyldimethylsilyloxy)pregna-5,7-dien-20(S)-yl}oxy]acetic acid (91 mg, 0.147 mmol) was treated with 3-pentanol (39 mg, 0.443 mmol), N,N′-dicyclohexylcarbodiimide (61 mg, 0.296 mmol) and 4-(dimethylamino)pyridine (54 mg, 0.443 mmol) in dichloromethane (1.5 ml) in the same manner as shown in Example 17(3) (at room temperature for 15 hours), followed by work up and purification using preparative thin layer chromatography (0.5 mm×3 plates, hexane:ethyl acetate=5:1, developed once) to give the titled compound (37 mg, 37%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985744B2
Source datasetuspto-grants-2011_07
ORD IDord-b118c2ada1f94fbe8ae910cf524d63eb
Source noteuspto-grants-2011_07