Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277160Generated: October 31, 2026

Triphenylphosphine → tert-butyl ((2S)-1-((2-(3-chloro-4-(cyclopropylmethoxy)phenyl)-1,3-benzoxazol-6-yl)oxy)propan-2-yl)carbamate

https://huagongshe.com/reaction/2277160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1,1-Dimethylethyl N-((1S)-2-hydroxy-1-methylethyl)carbamateHCID 7023103—
ReactantDIAD tolueneHCID 66880968—
Reactant2-(3-Chloro-4-(cyclopropylmethoxy)phenyl)-1,3-benzoxazol-6-olHCID 86731212—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl ((2S)-1-((2-(3-chloro-4-(cyclopropylmethoxy)phenyl)-1,3-benzoxazol-6-yl)oxy)propan-2-yl)carbamateHCID 8673121372.8%

Reaction Steps

To a solution of 2-(3-chloro-4-(cyclopropylmethoxy)phenyl)-1,3-benzoxazol-6-ol (1.00 g), tert-butyl ((2S)-1-hydroxypropan-2-yl)carbamate (0.832 g) and triphenylphosphine (1.25 g) in THF (10 mL) was added dropwise diisopropyl azodicarboxylate toluene solution (1.9 M, 2.50 mL), and the mixture was stirred at room temperature for 16 hr. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (NH, hexane/ethyl acetate) to give the title compound (1.09 g). 1H NMR (300 MHz, CDCl3) δ 0.39-0.48 (2H, m), 0.61-0.76 (2H, m), 1.14-1.37 (4H, m), 1.46 (9H, s), 3.90-4.04 (4H, m), 4.03-4.19 (1H, m), 4.77 (1H, brs), 6.95 (1H, dd, J=8.7, 2.3 Hz), 7.01 (1H, d, J=8.7 Hz), 7.10 (1H, d, J=2.3 Hz), 7.60 (1H, d, J=8.7 Hz), 8.04 (1H, dd, J=8.5, 2.1 Hz), 8.22 (1H, d, J=1.9 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133129B2
Source datasetuspto-grants-2015_09
ORD IDord-3831ce0170214cd6addd28689b7ff5ae
Source noteuspto-grants-2015_09