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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527316Generated: November 4, 2026

3-(Trifluoromethoxy)aniline → HCID 68283302, compound

https://huagongshe.com/reaction/1527316

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethoxy)anilineHCID 73753—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant(2S)-1-((tert-butoxy)carbonyl)-4-methylidenepyrrolidine-2-carboxylic acidHCID 21727417—
SolventDichloromethaneHCID 6344—
ProductHCID 68283302HCID 68283302—

Reaction Steps

To a suspension of N-Boc-4-methylene-L-proline (1 g, 4.4 mmol) in CH2Cl2 (40 mL) was added 3-(trifluoromethoxy)aniline (0.71 mL, 5.28 mmol), HBTU (1.14 g, 6.6 mmol) and diisopropylethylamine (1.51 mL, 8.8 mmol). The reaction mixture was stirred at RT for 2 days. The mixture was successively washed with 30 mL of a saturated aqueous NaHCO3 solution and an HCl 1M solution. The organic layers were dried (phase separator) and concentrated under vacuum. The crude residue was purified by flash column chromatography on silica gel (eluent: c-hexane/EtOAc:65/35) to give the title compound. TLC, Rf (c-hexane/EtOAc: 1:1)=0.55; MS (LC/MS): 287.0 [M-Boc]+, 385.0 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085555B2
Source datasetuspto-grants-2015_07
ORD IDord-7fa72203b64e4938ae851a8b0554ed72
Source noteuspto-grants-2015_07