Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456434Generated: October 29, 2026

2-Bromophenol → HCID 69418362, compound

https://huagongshe.com/reaction/456434

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromophenolHCID 7244—
ReactantTriphenylphosphineHCID 11776—
Reactant1-Boc-3-hydroxypiperidineHCID 545699—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69418362HCID 6941836234%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ortho-bromophenol (1.72 g, 9.92 mmol) and racemic Boc-3-hydroxypiperidine (2 g, 9.92 mmol) were placed in THF (60 mL) with triphenylphosphine (3.9 g, 14.9 mmol), and the mixture was cooled to 0° C. DIAD (2.94 mL, 14.9 mmol) was added portion wise over 30 minutes, and the mixture was warmed to r.t. and stirred for about 16 hours. The mixture was diluted with ether (200 mL) and water was added (100 mL). The mixture was washed with 5N NaOH (100 mL), extracted with ether and concentrated. Ethyl acetate/hexanes was added, and the triphenylphosphine oxide was crystallized and filtered away. The residue was chromatographed on silica gel (ethyl acetate/hexanes) to afford the product (1.2 g, 34%) as a clear oil. MS found: 256.0 (M-Boc)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186715B2
Source datasetuspto-grants-2007_03
ORD IDord-f03264f844d64879bc4c8c6d7d27d7f8
Source noteuspto-grants-2007_03