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

Hydrochloric Acid → 6-(Hydroxymethyl)-2-benzofuran-1(3H)-one

HRID 2080899
Notes
Print preview

Reaction equation

HRID 2080899 reaction equation
C[O:2][C:3](=[O:14])[C:4]1[CH:9]=[C:8]([CH2:10]Br)[CH:7]=[CH:6][C:5]=1[CH2:12]Br.C(=O)([O-])[O-:16].[Ca+2].Cl>O1CCOCC1>[OH:16][CH2:10][C:8]1[CH:9]=[C:4]2[C:5]([CH2:12][O:2][C:3]2=[O:14])=[CH:6][CH:7]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 10112Calcium CarbonateHCID 12633556Methyl 2,5-bis(bromomethyl)benzoate

Product 1

HCID 178625846-(Hydroxymethyl)-2-benzofuran-1(3H)-one

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Conditions

Temperature
100 °C

Procedure

The compound (1.1274 g) obtained in Example 102-1 was dissolved in carbon tetrachloride (19.2 ml). The reaction solution was added with N-bromosuccinimide (2.417 g) and benzoyl peroxide (147.2 mg), and the whole was refluxed under heating for 6.5 hours. After having been cooled to room temperature, the reaction solution was concentrated under reduced pressure. The resultant residue was purified through silica gel column chromatography (hexane/ethyl acetate), thereby obtaining a mixture (2.4003 g) containing 2,5-bis-bromomethyl-benzoic acid methyl ester. The resultant mixture was dissolved in a 50% 1,4-dioxane aqueous solution (48 ml). The reaction solution was added with calcium carbonate (3.4823 g) and the whole was stirred at 100° C. for 16.5 hours. After having been cooled to room temperature, the reaction solution was cooled to 0° C. and concentrated hydrochloric acid was gradually added thereto to make the pH of the solution to 2. After that, the whole was stirred at room temperature for 20 minutes. The reaction solution was subjected to extraction with ethyl acetate. The organic layer was washed with a saturated aqueous sodium hydrogen carbonate solution and a saturated saline solution and then dried with anhydrous sodium sulfate. After the drying agent was filtrated out, the filtrate was concentrated under reduced pressure. The resultant residue was purified through silica gel column chromatography (chloroform/ethyl acetate), thereby obtaining the subject compound (372.0 mg) as a white crystal.

Workup

  1. temperatureAfter having been cooled to room temperature
  2. temperaturethe reaction solution was cooled to 0° C.
  3. stirringAfter that, the whole was stirred at room temperature for 20 minutes
  4. extractionThe reaction solution was subjected to extraction with ethyl acetate
  5. washThe organic layer was washed with a saturated aqueous sodium hydrogen carbonate solution
  6. dry with materiala saturated saline solution and then dried with anhydrous sodium sulfate
  7. filtrationAfter the drying agent was filtrated out
  8. concentrationthe filtrate was concentrated under reduced pressure
  9. customThe resultant residue was purified through silica gel column chromatography (chloroform/ethyl acetate)

Sources & evidence

ORD record
ord-dd8b359fd6704c9a804b253937db5d7d
Source dataset
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07932281B2

Reaction notes

Loading…

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes