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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279946Generated: October 31, 2026

Dichloromethane → HCID 14940799, compound

https://huagongshe.com/reaction/1279946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant3-NitrophenolHCID 11137—
ReactantAmmonium ChlorideHCID 25517—
ReactantPivaloyl chlorideHCID 62493—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
ProductHCID 14940799HCID 1494079994%

Reaction Steps

To 300 mL of CH2Cl2 was added 3-nitrophenol (structure 64 of Scheme XVII, where R1=H, Y=O) (15 g, 0.11 mol), pyridine (20 mL) and DMAP (10 mg). To this cooled solution (0° C.) was slowly added trimethylacetyl chloride (18 mL, 146 mmol, 1.4 equivuiv). The solution was allowed to warm to rt and stirred for 3 h. To the amber colored solution was added sat'd NH4Cl (300 mL). The organic layer was washed with 1N HCl (2×150 mL), 10% CuSO4. 5 H2O (2×100 mL), and brine (2×100 mL). The extract was dried (Na2SO4) and concentrated in vacuo to give 22.5 g (94%) of O-pivaloyl-3-nitrophenol as a white solid. Data for O-pivaloyl-3-nitrophenol: Rf 0.55 (silica gel, hexanes/EtOAc, 3:1); 1H NMR (400 MHz, CDCl3) 8.11 (dd, J=4.2, 1.3, 1H), 7.96 (t, J=2.2, 1H), 7.56 (dd, J=8.4, 8.2, 1H), 7.42 (dd, J=6.5, 1.3, 1H), 1.35 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448405B1
Source datasetuspto-grants-2002_09
ORD IDord-2a9494ddd4874de4b496460d973a182b
Source noteuspto-grants-2002_09