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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296753Generated: October 31, 2026

o-Phenylbenzoic acid → HCID 18387431, compound

https://huagongshe.com/reaction/2296753

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-Phenylbenzoic acidHCID 70357—
ReactantN,O-bis(trimethylsilyl)acetamideHCID 6913588—
Reactant[1,1'-Biphenyl]-2-carbonyl chlorideHCID 12563768—
ReactantHCID 18387440HCID 18387440—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18387431HCID 1838743183%

Reaction Steps

To a cold (ice-bath) solution of 2-(2-hydroxyethyl)-5-(4-aminobenzyl)-1,5-benzothiazepine-4-one as prepared in Example 21 (0.865 g, 2.6 mM) in dry THF was added N,O-bis(trimethylsilyl)acetamide (1.16 ml, 5.2 mM). After 1 hour, 2-phenylbenzoyl chloride (0.570 g, 2.6 mM), prepared from 2-biphenylcarboxylic acid as described in Example 3, was added and stirring was continued for an addition hour. Water (80 ml) was added and the mixture was extracted with ethyl acetate (2×80 ml). The organic extract was dried (MgSO4), filtered and evaporated in vacuo to give a crude product. Purification by flash column chromatography (EM silica gel 60; 30% EtOAc in CH2Cl2) yielded the desired product as a white solid (1.1 g, 83%) m.p.116-120° C. 1H NMR (300 MHz, DMSOd6) δ7.8 (d, J=7 Hz, 1H); 5.09(d, J=15 Hz, H); 4.89(d,J=15 Hz,1H); 3.79 (m, 3H); 2.69-2.24(m, 2H); 1.71 (m, 2H); m/z (MH+)509.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06489321B1
Source datasetuspto-grants-2002_12
ORD IDord-e89c51fcff88484b8c00ce3448989f65
Source noteuspto-grants-2002_12