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Benzyl Alcohol → Benzyl mesylate

HRID 614562
Notes
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Reaction equation

HRID 614562 reaction equation
[CH2:1]([OH:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.[CH3:16][S:17](Cl)(=[O:19])=[O:18]>ClCCl>[CH3:16][S:17]([O:8][CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)(=[O:19])=[O:18]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 244Benzyl AlcoholHCID 8471TriethylamineHCID 31297Methanesulfonyl chloride

Product 1

HCID 148757Benzyl mesylate

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

To an ice cooled solution of 54 g (0.5 mol) of benzyl alcohol and 75.75 g (104.3 ml, 0.75 mol) of triethylamine in 1800 ml of dichloromethane is added dropwise 63 g (42.57 ml, 0.55 mol) of methanesulfonyl chloride. The temperature of the reaction mixture during the addition is ca. 10°. The reaction mixture is then stirred for 1.5 hours at 10°. The reaction mixture is then diluted with dichloromethane, washed with ice water, cold 10% HCl, saturated KHCO3, saturated NaCl and dried (MgSO4). Solvent is removed in vacuo to yield the benzyl methanesulfonate as an oil.

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. additionThe temperature of the reaction mixture during the addition
  2. customis ca. 10°
  3. washwashed with ice water, cold 10% HCl, saturated KHCO3, saturated NaCl
  4. dry with materialdried (MgSO4)
  5. customSolvent is removed in vacuo

Sources & evidence

ORD record
ord-142440ae98ad4ede98e4142a5d04f31d
Source dataset
uspto-grants-1979_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04145433

Reaction notes

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