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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641619Generated: November 2, 2026

2,2,4-Trimethylpentane → HCID 57543426, compound

https://huagongshe.com/reaction/1641619

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,4-TrimethylpentaneHCID 10907—
Reactanto-Phenylbenzoic acidHCID 70357—
ReactantDichloromethane ethylacetateHCID 21226138—
ProductHCID 57543426HCID 57543426—

Reaction Steps

Palladium acetate (5.6 mg, 0.025 mmol), 2-phenylbenzoic acid (99 mg, 0.5 mmol) and 3,5-dimethylchlorobenzene (211 mg, 1.5 mmol), butyldi-1-adamantylphosphine (19.2 mg, 0.05 mmol), Cs2CO3 (358 mg, 1.1 mmol), molecular sieves 3 Å (155 mg and anhydrous DMF (2.5 mL). After flash chromatography and preparative HPLC 101 mg (67%) of a white solid was obtained, mp 198-200° C. (isooctane). Rf-0.79 (1/9 ethyl acetate-dichloromethane). 1H NMR (300 MHz, CDCl3) δ 2.30 (s, 6H), 7.00 (s, 1H), 7.03 (s, 2H), 7.33-7.38 (m, 7H), 7.46-7.52 (m, 1H), 9.6 (br s, 1H). 1C NMR (75 MHz, CDCl3) δ 21.7, 122.5, 126.9, 128.1, 128.8, 129.0, 129.3, 129.5, 129.8, 130.0, 132.0, 138.3, 140.7, 141.0, 141.2, 174.2. FT-IR (neat, cm1) υ 1688, 1295. Anal. calcd for C21H18O2 (302.37 g/mol): C, 83.42; H, 6.00. Found: C, 83.13; H, 6.05. The 1H NMR spectrum of 2-phenylbenzoic acid is shown in FIG. 41. The 1H NMR and 13C NMR spectra of the product are shown in FIGS. 42A&E, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114993B2
Source datasetuspto-grants-2012_02
ORD IDord-61713dfd5b3a4bd59a15f036ae8908da
Source noteuspto-grants-2012_02