Water → HCID 54490045, compound

HRID 864991Notes

Reaction equation

HRID 864991 reaction equation
[C:1]([O:20][CH2:21][CH:22]([CH2:25][CH2:26][OH:27])[CH2:23][OH:24])([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N([CH2:33][CH3:34])CC)C.[C:35](Cl)(=[O:37])[CH3:36].[OH2:39]>C(OCC)C>[C:35]([O:24][CH2:23][CH:22]([CH2:21][O:20][C:1]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)([C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)[CH2:25][CH2:26][O:27][C:33](=[O:39])[CH3:34])(=[O:37])[CH3:36]

Participants

6

Reactant 4

HCID 962WaterHCID 6367Acetyl chlorideHCID 8471TriethylamineHCID 19027592HCID 19027592, compound

Product 1

HCID 54490045HCID 54490045, compound

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent2×

Procedure

To a stirred mixture of 2-trityloxymethyl-1,4-butandiol (50.85 g, 0.140 mol) and triethylamine (42.6, 0.42 mol) in dry diethyl ether (500 ml) was added slowly a solution of acetyl chloride (27.5 g 0.35 mol) in ether (25 ml) with external cooling with cold water to maintain room temperature in the mixture. After 45 min the triethylamine hydrochloride was filtered off and washed with a little ether. The combined filtrate was washed with water (50 ml), 0.5M hydrochloric acid (100 ml) and water (50 ml), dried with magnesium sulfate and evaporated in vacuum, finally at 0.1 mBar, to give 61.03 g (97%) of crude oily product. TLC on silica (ethyl aceteate+n-hexane 1+1): Rf 0.68.

Workup

  1. filtrationAfter 45 min the triethylamine hydrochloride was filtered off
  2. washwashed with a little ether
  3. washThe combined filtrate was washed with water (50 ml), 0.5M hydrochloric acid (100 ml) and water (50 ml)
  4. dry with materialdried with magnesium sulfate
  5. customevaporated in vacuum, finally at 0.1 mBar
  6. customto give 61.03 g (97%) of crude oily product

Sources & evidence

ORD record
ord-cd849bcc589f4b27ad9364e3b9f13bb2
Source dataset
uspto-grants-1996_10
Patent number
US05565461

Reaction notes

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