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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468657Generated: October 31, 2026

Nitrogen → HCID 70980523, compound

https://huagongshe.com/reaction/1468657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
Reactant1,2-DibromoethaneHCID 7839—
ReactantTriphenylphosphineHCID 11776—
Reactanttert-butyl N-(2-hydroxyethyl)carbamateHCID 2733206—
ReactantDiethyl azodicarboxylateHCID 5462977—
ReactantHCID 84662442HCID 84662442—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 70980523HCID 7098052370%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of triphenylphosphine (1.9 g, 7.3 mmol) in dry THF (20 ml) was flushed with N2(g) and DEAD (3.1 ml, 6.9 mmol) was added drop-wise, 1,2-dibromoethane followed by 3-fluoro-5-methylsulfonyl-phenol (1.1 g, 6.1 mmol) and then boc-glycinol (1.0 ml, 6.1 mmol) in portions. The mixture was stirred at 70° C. for 20 h, cooled to room temperature and water and EtOAc was added. The aqueous phase was extracted with ethyl acetate (2×100 ml). The combined organic phase was washed with aqueous NaOH (3 M, 50 ml) and brine (75 ml), dried (Na2SO4) and evaporated. Purification by flash column chromatography (ethyl acetate/isooctane, 0:1 to 1:0) gave the title compound (1.4 g, 70%). MS m/z (relative intensity, 70 eV 298 (M+, 18), 296 (M+, 18), 109 (bp), 107 (99), 82 (15).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006227B2
Source datasetuspto-grants-2015_04
ORD IDord-1ffac7e148bc42e79a1387ad81e3a849
Source noteuspto-grants-2015_04