HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Acetone → 1,2,10-Decanetriol

HRID 54580
Notes
Print preview

Reaction equation

HRID 54580 reaction equation
[CH2:1]([OH:11])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7]CC=C.[CH3:12][C:13]([CH3:15])=[O:14].C[N+]([O-:20])(C)C.S(=O)(O)[O-].[Na+]>C(O)(C)(C)C.[Os](=O)(=O)(=O)=O.O>[CH2:12]([OH:20])[CH:13]([OH:14])[CH2:15][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][CH2:1][OH:11]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 4

HCID 180AcetoneHCID 1145Trimethylamine oxideHCID 256129-Decen-1-olHCID 23665763Sodium Bisulfite

Product 1

HCID 27359121,2,10-Decanetriol

Reagents, catalysts & solvents 3

HCID 30318Osmium TetroxideCatalyst
HCID 962
Water
Solvent
HCID 6386tert-ButanolSolvent2×

Procedure

9-Decen-1-ol (25.0 g, 160 mmol) was dissolved in a solution made up of t-butanol (100 ml), acetone (90 ml) and water (10 ml). To this solution was added trimethylamine-N-oxide (26.6 g, 240 mmol) and 2 ml of a solution of osmium tetroxide (500 mg) in t-butanol (25 ml). The resulting solution was stirred 20 hours under nitrogen then 10% sodium bisulfite was added (50 ml). The mixture was concentrated, then taken up in trichloromethane and washed 2 times with water, dried with Na2SO4 and concentrated to give 1,2,10-decanetriol as an oil. This material was used without further purification in preparation of the corresponding acetonide (of formula 21).

Workup

  1. concentrationThe mixture was concentrated
  2. washwashed 2 times with water
  3. dry with materialdried with Na2SO4
  4. concentrationconcentrated

Sources & evidence

ORD record
ord-31a1e74b8fe943d6bdee245abc523527
Source dataset
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05622712

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes