4-Hydroxybenzoic Acid → 4-(2-Bromoethoxy)-4'-hydroxybenzophenone

HRID 2082565

Reaction equation

HRID 2082565 reaction equation
[O:1]([CH2:8][CH2:9][Br:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH:11][C:12]1[CH:20]=[CH:19][C:15]([C:16](O)=[O:17])=[CH:14][CH:13]=1>>[Br:10][CH2:9][CH2:8][O:1][C:2]1[CH:7]=[CH:6][C:5]([C:16]([C:15]2[CH:19]=[CH:20][C:12]([OH:11])=[CH:13][CH:14]=2)=[O:17])=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 1354-Hydroxybenzoic AcidHCID 68526Benzene, (2-bromoethoxy)-

Product 1

HCID 127097874-(2-Bromoethoxy)-4'-hydroxybenzophenone

Procedure

Melting points (mp) were obtained on a capillary melting point apparatus and are uncorrected. Elemental analyses of all compounds prepared were within ±0.4% of calculated theoretical values. Reaction progress and purity of products were checked by analytical TLC using 0.2 mm silica gel plastic backed layers, and viewed under light of 254 nm wavelength. Proton NMR spectra were obtained at 90 mHz and EIMS were obtained using a direct ion probe. 4-(2-Bromoethoxy)-4'-hydroxybenzophenone was prepared by acylation of 2-phenoxyethyl bromide with 4-hydroxybenzoic acid: mp 136°-138° C.

Workup

  1. customMelting points (mp) were obtained on a capillary
  2. customElemental analyses of all compounds prepared
  3. customReaction progress and purity of products
  4. customProton NMR spectra were obtained at 90 mHz
  5. customEIMS were obtained

Sources & evidence

ORD record
ord-55caa1af954947a0b9de6fd6d70f5be3
Source dataset
uspto-grants-1993_02
Patent number
US05189212

Linked notes

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