Hydrochloric Acid → 5,5-Bis(bromomethyl)-1,3-dioxane

HRID 1608136Notes

Reaction equation

HRID 1608136 reaction equation
[Br:1][CH2:2][C:3]([CH2:8][Br:9])([CH2:6][OH:7])[CH2:4][OH:5].Cl.[CH2:11]=O>>[Br:1][CH2:2][C:3]1([CH2:8][Br:9])[CH2:6][O:7][CH2:11][O:5][CH2:4]1

Participants

4

Conditions

Temperature
50 °C

Procedure

A suspension of 26.2 g of 2,2-bis(bromomethyl)-1,3-propanediol, 50 ml of concentrated hydrochloric acid and 50 ml of 38% formaldehyde was stirred in a 50° C. oil bath overnight, then cooled to room temperature and filtered. The filtrate was extracted with three 100 ml portions of ether. The ether extracts were combined, washed with water, dried and evaporated to an oil. A small amount of solid which formed was removed by filtration and washing with ether. The filtrate and wash were evaporated under reduced pressure, giving 26.9 g of 5,5-bis(bromomethyl)-1,3-dioxane as a clear oil.

Workup

  1. temperaturecooled to room temperature
  2. filtrationfiltered
  3. extractionThe filtrate was extracted with three 100 ml portions of ether
  4. washwashed with water
  5. customdried
  6. customevaporated to an oil
  7. customA small amount of solid which formed
  8. customwas removed by filtration
  9. washwashing with ether
  10. washThe filtrate and wash
  11. customwere evaporated under reduced pressure

Sources & evidence

ORD record
ord-0eff4193407f447abb43259b812391db
Source dataset
uspto-grants-1989_09
Patent number
US04870070

Reaction notes

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