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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944832Generated: October 30, 2026

t-Butyl carbanilate → HCID 178506929, compound

https://huagongshe.com/reaction/1944832

Reaction equation

Participants

RoleNameHCIDCharge
Reactantt-Butyl carbanilateHCID 137930—
ReactantButyllithiumHCID 178418339—
SolventPentaneHCID 8003—
ProductHCID 178506929HCID 17850692977.4%

Reaction Steps

Pentane (350 mL) was added to tert-butyl phenylcarbamate (20.81 g, 107.7 mmol) to form a suspension. BuLi (67.3 mL, 107.7 mmol) in hexanes was added dropwise over 1 hour. During the addition a clear solution formed briefly then a white precipitate formed. After the addition was complete the mixture was stirred for 1 hour then the solid was collected on a glass frit, washed with pentane (2×20 mL), and dried under reduced pressure to afford LiN(Boc)Ph (16.6 g, 77.4%). 2-Bromomethylphenyl boronic acid pinacol ester (compound 9) (4.66 g, 15.7 mmol) and N,N-dimethylformamide (DMF) (35 mL) were combined to form a clear colorless solution. Then solid LiN(Boc)Ph (3.13 g, 15.7 mmol) was added in small portions over three minutes. The mixture was stirred for 2 hours then the white suspension was poured into water (250 mL). Et2O (150 mL) was added and the organics were separated, dried with brine then magnesium sulfate. Filtration followed by evaporation afforded the product as a white solid. 1H NMR (CDCl3, 250 MHz): 7.77 (d, 1H), 7.0-7.5 (m, 8H), 5.19 (s, 2H), 1.39 (s, 9H), 1.27 (s, 12H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394902B2
Source datasetuspto-grants-2013_03
ORD IDord-166b48a73967493fbb5c5107f7af27d7
Source noteuspto-grants-2013_03