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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070395Generated: November 3, 2026

Dicyclohexylcarbodiimide → HCID 69687087, compound

https://huagongshe.com/reaction/1070395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-Hydroxy-1-naphthoic acidHCID 16790—
Reactant2-(Trimethylsilyl)ethanolHCID 18013—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69687087HCID 6968708794.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-hydroxynaphtoic acid (2.02 g, 10.7 mmol) in dichloromethane (45 mL) and THF (2 mL) were added 2-trimethylsilylethanol (4.6 mL, 32.2 mmol) and 4-dimethylaminopyridine (1.07 g, 8.9 mmol) under N2. The mixture was cooled to 0° C. and 1,3-dicyclohexylcarbodiimide (2.33 g, 11.3 mmol) was added. After removal of the ice bath, the mixture was stirred for 3 h at room temperature. 2N HCl was added to adjust the pH to 2, and the mixture was filtered to remove urea. After the separation of layers the organic phase was washed with water and brine, dried (Na2SO4), and concentrated to dryness. Purification by chromatography gave 2.92 g of 2-hydroxy-naphthalene-1-carboxylic acid 2-trimethylsilanyl-ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903086B2
Source datasetuspto-grants-2005_06
ORD IDord-43b2f5c91b0c43b89fb95dcde4bff127
Source noteuspto-grants-2005_06