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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034579Generated: October 30, 2026

2-Naphthol → HCID 58922276, compound

https://huagongshe.com/reaction/1034579

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NaphtholHCID 8663—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantHCID 66917356HCID 66917356—
SolventDichloromethaneHCID 6344—
ProductHCID 58922276HCID 5892227664%

Reaction Steps

5 g of 2-hydroxycarbonylmethyl-4(R)-tetrahydropyranyloxy-2-cyclopenten-1-one (21 mmol) obtained from Example 44, 2-naphthol (4.7 g, 32 mmol), dichloromethane (50 ml), and 0.2 g 4-(dimethylamine)pyridine were added together to a 50 ml dichloromethane solution containing 1,3-dicyclohexylcarbodiimide (7 g, 34 mmol). The reaction mixture was stirred at room temperature for about 4 hours. The precipitate was filtered off. The filtrate was washed with 20 ml of diluted hydrochloride solution, water, dried over anhydrous magnesium sulfate, filtered, and evaporated under vacuum. The residue was purified by flash chromatography on silica gel to give the titled compound as white solid (3.8g, 64%). MP: 75° C.; [α]D+29.3° (c 1.0, CH3CN); 1H-NMR (CDCl3/TMS): δ 7.10˜7.90 (m, 8H), 4.72˜5.11 (m, 2H), 3.90 (m, 1H), 3.60 (m, 3H), 2.89 (m, 1H), 2.35˜2.60 (m, 1H), 1.40˜1.92 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546114B2
Source datasetuspto-grants-2013_10
ORD IDord-5bb7e58f5c3942f89109f5222ca301db
Source noteuspto-grants-2013_10