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Hydrochloric Acid → 2-(3-(Hydroxymethyl)phenylthio)ethanol

HRID 446381
Notes
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Reaction equation

HRID 446381 reaction equation
CSC.B.[Si]([O:12][CH2:13][CH2:14][S:15][C:16]1[CH:17]=[C:18]([CH:22]=[CH:23][CH:24]=1)[C:19](O)=[O:20])(C(C)(C)C)(C)C.Cl>C1COCC1>[OH:20][CH2:19][C:18]1[CH:17]=[C:16]([S:15][CH2:14][CH2:13][OH:12])[CH:24]=[CH:23][CH:22]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 12423031(Dimethyl sulfide)trihydroboronHCID 579893363-(2-(tert-Butyldimethylsilyloxy)ethylthio)benzoic acid

Product 1

HCID 579893042-(3-(Hydroxymethyl)phenylthio)ethanol

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

Borane dimethyl sulfide complex (2M in THF, 17.3 mL) was added dropwise to an ice cold solution of 3-(2-(tert-butyldimethylsilyloxy)ethylthio)benzoic acid [Aromatic Intermediate 16, step a] (2.16 g) in THF (50 mL). The reaction was allowed to warm to RT, then heated at reflux for 2 h. The reaction was cooled in an ice bath and aqueous HCl solution (2M, 50 mL) was added dropwise. The resulting mixture was stirred overnight. The reaction was concentrated to half its original volume and the resulting aqueous extracted with DCM (3×100 mL). The combined organics were washed with brine (100 mL), dried over sodium sulphate, filtered and evaporated. The residue was purified by silica gel chromatography eluting with 4:1 isohexane:ethyl acetate to 100% ethyl acetate gradient. The fractions containing product were combined and evaporated to give the subtitled compound as a clear oil. Yield 0.77 g.

Workup

  1. temperatureheated
  2. temperatureat reflux for 2 h
  3. temperatureThe reaction was cooled in an ice bath
  4. concentrationThe reaction was concentrated to half its original volume
  5. extractionthe resulting aqueous extracted with DCM (3×100 mL)
  6. washThe combined organics were washed with brine (100 mL)
  7. dry with materialdried over sodium sulphate
  8. filtrationfiltered
  9. customevaporated
  10. customThe residue was purified by silica gel chromatography
  11. washeluting with 4:1 isohexane
  12. additionThe fractions containing product
  13. customevaporated

Sources & evidence

ORD record
ord-dc2c4062b5b3455c9582e0bd62ae52a0
Source dataset
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08476265B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes