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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747886Generated: October 30, 2026

Triphenylphosphine → HCID 66849850, compound

https://huagongshe.com/reaction/747886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantN-(Triphenylmethyl)-L-serine methyl esterHCID 7128367—
ReactantN-Cbz4-(4-hydroxyphenyl)butylamineHCID 11637991—
SolventBenzeneHCID 241—
ProductHCID 66849850HCID 6684985064.7%

Reaction Steps

Commercially available N-trityl-L-serine methyl ester (1.60 g, 5.34 mmol) was combined with triphenylphosphine (1.28 g, 4.88 mmol) and [4-(4-hydroxyphenyl)butyl]carbamic acid benzyl ester (2.0 g, 6.68 mmol) in benzene (40 mL) at room temperature. Diisopropyl azodicarboxylate (0.958 mL, 4.86 mmol) was added dropwise and the reaction was stirred for 14 days. The solvent was removed under reduced pressure and the residue was purified by column chromatography (silica gel, eluent: 6:1, v/v dichloromethane/ethyl acetate) to provide compound 10 (2.22 g, 51%). 1H NMR (300 MHz, CDCl3) δ 7.52 (m, 6H), 7.39-7.14 (m, 14H), 7.06 (d, 2H), 6.79 (d, 2H), 5.09 (s, 2H), 4.72 (m, 1H), 4.24 (m, 1H), 4.01 (m, 1H), 3.72 (m, 1H), 3.22 (s, 3H), 3.18 (m, 2H), 2.88 (d, 1H), 2.57 (m, 2H), 1.66-1.48 (m, 4H). Rf=0.91 (5:1 v/v dichloromethane/ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399766B2
Source datasetuspto-grants-2008_07
ORD IDord-232fb7ef3f2d4d3193cd9c47fa88bbe8
Source noteuspto-grants-2008_07