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Hydrochloric Acid → 2-(3-Bromobenzyloxy)ethanol

HRID 658900
Notes
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Reaction equation

HRID 658900 reaction equation
CC(C[AlH]CC(C)C)C.[Br:10][C:11]1[CH:12]=[C:13]([CH:17]2[O:21][CH2:20][CH2:19][O:18]2)[CH:14]=[CH:15][CH:16]=1.Cl>CCCCCCC>[Br:10][C:11]1[CH:12]=[C:13]([CH:14]=[CH:15][CH:16]=1)[CH2:17][O:18][CH2:19][CH2:20][OH:21]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 14487Diisobutylaluminum hydrideHCID 873062-(3-Bromophenyl)-1,3-dioxolane

Product 1

HCID 579568182-(3-Bromobenzyloxy)ethanol

Reagents, catalysts & solvents 1

HCID 8900HeptaneSolvent

Procedure

A solution of DIBAL-H in heptane is added under an inert atmosphere to a cooled (−78° C.) solution of 2-(3-bromophenyl)-1,3-dioxolane in hexanes. The reaction mixture is stirred until no starting material is seen by TLC. Aqueous HCl (1N) is added to the reaction mixture while warming to room temperature. The product is extracted with EtOAc. Combined organic layers are dried over anhydrous MgSO4, and concentrated under reduced pressure to give 2-(3-bromobenzyloxy)ethanol.

Workup

  1. extractionThe product is extracted with EtOAc
  2. dry with materialCombined organic layers are dried over anhydrous MgSO4
  3. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-d6290984b23c4033b0818dc1a9a1c022
Source dataset
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08076516B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes