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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389100Generated: November 1, 2026

Tetrahydrofuran → HCID 178445733, compound

https://huagongshe.com/reaction/2389100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant(R)-4-(6-hydroxy-5-(trifluoromethyl)naphthalen-2-yl)-4-methyloxazolidin-2-oneHCID 46196301—
ReactantHCID 178445811HCID 178445811—
SolventDichloromethaneHCID 6344—
ProductHCID 178445733HCID 17844573330.5%

Reaction Steps

The mixture of cis-4-tert-butylcyclohexanol (30.4 mg, 0.000195 mol), (R)-4-(6-hydroxy-5-(trifluoromethyl)naphthalen-2-yl)-4-methyloxazolidin-2-one (50.5 mg, 0.000162 mol) and triphenylphosphine (51.1 mg, 0.000195 mol) in tetrahydrofuran (2 mL, 0.02 mol) was heated to reflux, and diisopropyl azodicarboxylate (0.0383 mL, 0.000195 mol) was added dropwise and was stirred and refluxed for 3 hours. The mixture was taken up into methylene chloride and subjected to chromatography purification with EtOAc/hexane (10:90 to 80:20) to give product (R)-4-(6-(trans-4-tert-butylcyclohexyloxy)-5-(trifluoromethyl)naphthalen-2-yl)-4-methyloxazolidin-2-one (22.2 mg, 30%). LCMS: Rf=2.41 min (450.46, M+1, 70%; 491.47, M+ACN, 100%). 1H NMR (400 MHz, CHLOROFORM-d) δ=8.25 (dd, J=8.7, 1.4 Hz, 1 H), 7.91 (d, J=9.0 Hz, 1 H), 7.79 (d, J=2.0 Hz, 1 H), 7.52 (dd, J=9.3, 2.3 Hz, 1 H), 7.34 (d, J=9.3 Hz, 1 H), 5.98 (br. s., 1 H), 4.45 (d, J=8.6 Hz, 1 H), 4.41 (d, J=8.6 Hz, 1 H), 4.38-4.26 (m, 1 H), 2.19 (d, J=13.1 Hz, 2 H), 1.89 (d, J=10.0 Hz, 2 H), 1.87 (s, 3 H), 1.59-1.48 (m, 2 H), 1.21-1.05 (m, 3 H), 0.89 (s, 9 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08269043B2
Source datasetuspto-grants-2012_09
ORD IDord-8126cb3dd4c74a08ab14d753fc6cb327
Source noteuspto-grants-2012_09