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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278805Generated: November 3, 2026

Triphenylphosphine → HCID 10169000, compound

https://huagongshe.com/reaction/1278805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant(S)-methyl 2-hydroxy-3-phenylpropanoateHCID 5289077—
ReactantDiethyl azodicarboxylateHCID 5462977—
ReactantHCID 9893519HCID 9893519—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
ProductHCID 10169000HCID 1016900097.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

Diethylazodicarboxylate (0.262 mL, 1.67 mmol) was added dropwise to a stirred, room temperature solution of 2,6-dibromo-4-(9-bromo-2,3-dimethyl-naphtho[2,3-b]thiophen-4-yl)-phenol (0.60 g, 1.11 mmol), and (S)-2-hydroxy-3-phenylpropionic acid, methyl ester (0.300 g, 1.67 mmol), triphenylphosphine (0.437 g, 1.67 mmol) and benzene (5 mL) and the solution was heated in an 80° C. oil bath for 6 h. Upon cooling to room temperature, the reaction mixture was diluted with ether and silica gel (30 mL) was added. The reaction mixture was concentrated and the silica adsorbate was flash chromatographed (95:5 petroleum ether:ethyl acetate) to provide the title compound as a white solid (0.76 g, 97%): mp 174-175° C.: NMR (DMSO-d6); δ 8.21 (ddd, J=8,1,1 Hz, 1H), 7.74 (d, J=2 Hz, 1H), 7.73 (d, J=2 Hz, 1H),7.67 (ddd, J=8, 6, 1 Hz, 1H), 7.53 (ddd, J=8, 7, 1 Hz, 1H), 7,43 (d, J=8 Hz, 1H), 7.35-7.24 (m, 5H), 5.11 (dd, J=7, 6 Hz, 1H), 3.61 (s, 3H), 3.43 (dd, 13, 6 Hz, 1H), 3.40 (dd, 13, 7 Hz, 1H), 2.44 (d, J=1 Hz, 3H), 1.60 (d, J=1 Hz, 3H); MS (+FAB): 3 bromine isotope pattern 700(20%), 702 (70%), 704 (75%), 706 (25%); Anal. Calc. for C30H23Br3O3S: C, 51.23, H, 3.30, N, 0.00. Found: C, 51.52, H, 3.36, N, 0.12.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06444670B2
Source datasetuspto-grants-2002_09
ORD IDord-a1350fe94c24424ca18638393f89f5b6
Source noteuspto-grants-2002_09