Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132243Generated: October 26, 2026

Pivaloyl chloride → N-(4,5-Difluoro-2-(hydroxymethyl)phenyl)pivalamide

https://huagongshe.com/reaction/132243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivaloyl chlorideHCID 62493—
ReactantDiisopropylethylamineHCID 81531—
Reactant(2-Amino-4,5-difluorophenyl)methanolHCID 21925570—
SolventTetrahydrofurane dichloromethaneHCID 21919333—
ProductN-(4,5-Difluoro-2-(hydroxymethyl)phenyl)pivalamideHCID 59732039—

Reaction Steps

Trimethylacetyl chloride (4.01 mL, 32.55 mmol) was added to the solution of the crude (2-amino-4,5-difluorophenyl) methanol in CH2Cl2/THF (50 mL/10 mL) at 0° C., followed by the addition of DIEA (10.8 mL, 62 mmol). The resulting mixture was stirred for 30 min, and then partitioned between saturated NaHCO3(100 mL) and CH2Cl2 (150 mL). After separation, the organic phase was washed with brine (40 mL), dried over MgSO4, and concentrated on rotary vacuum to afford the expected product, which was pure enough to be used in next step without further purification; 1H NMR (400 MHz, CDCl3) δ ppm 1.28 (s, 9 H), 4.62 (s, 2 H), 6.94 (dd, J=10.20, 8.44 Hz, 1 H), 8.08 (dd, J=12.72, 7.68 Hz, 1 H), 9.04 (s, 1 H); Mass spec. 244.11 (MH+), Calc. for C12H15F2NO2 243.11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384930B2
Source datasetuspto-grants-2008_06
ORD IDord-f103b7c4ac204e5582dfd67e17e3e220
Source noteuspto-grants-2008_06