Formaldehyde → HCID 14652260, compound

HRID 1087651Notes

Reaction equation

HRID 1087651 reaction equation
[CH2:1]=O.[CH2:3]([NH:5][CH2:6][CH3:7])[CH3:4].[CH2:8]([OH:13])[CH2:9][CH2:10][C:11]#[CH:12].[OH-].[K+]>O1CCOCC1>[CH2:3]([N:5]([CH2:6][CH3:7])[CH2:1][C:12]#[C:11][CH2:10][CH2:9][CH2:8][OH:13])[CH3:4]

Participants

6

Conditions

Temperature
60 °C

Procedure

A mixture of paraformaldehyde (7.14 g, 238 mmol), diethylamine (27.6 ml, 260 mmol) and cupric acetate monohydrate (1 g) in dioxane (40 ml) was heated in an oil bath of 60° C. for 1 hour. When the solid material disappeared, pent-4-yn-1-ol (20 g, 238 mmol) was added and the heating at 95° C. was continued until the greenish suspension had been completely replaced by the thin brown precipitate (approximately 3 hours). After cooling to 20° C., the reaction mixture was poured into 10% aqueous KOH (40 ml). The precipitate was filtered off and washed with ether (100 ml). The organic phase was washed with water (5 times 50 ml), dried (K2CO3) and evaporated to dryness to give crude product. The isolated product was distilled to yield 29.78 g (74%) of 6-diethylaminohex-4-yn-1-ol: bp 92°-94° C. (0.1 mm Hg), IR (neat) 3309 cm-1 ; 1H NMR (CDCl3) δ4.1(S, 1H), 3.6(t, 2H), 3.3(m, 2H), 2.7-2.0(m, 6H), 2.0-1.4(m, 2H), 1.0(t, 6H).

Workup

  1. customheating at 95° C.
  2. customhad been completely replaced by the thin brown precipitate (approximately 3 hours)
  3. temperatureAfter cooling to 20° C.
  4. filtrationThe precipitate was filtered off
  5. washwashed with ether (100 ml)
  6. washThe organic phase was washed with water (5 times 50 ml)
  7. dry with materialdried (K2CO3)
  8. customevaporated to dryness
  9. customto give crude product
  10. distillationThe isolated product was distilled

Sources & evidence

ORD record
ord-376f6bf1b3614627bbfdf0c515d4ce2b
Source dataset
uspto-grants-1991_07
Patent number
US05036107

Reaction notes

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