تفاعل #6056

ord-c6befcbde27c4bafadace118dde28422

معادلة التفاعل

[BH4-].[Na+]
Sodium borohydride
O=C(OC1CC(CO)C1=O)c1ccccc1
2-Benzoyloxy-4-hydroxymethylcyclobutanone
[BH4-]
borohydride
O=C(OC1CC(CO)C1O)c1ccccc1
title compound
المردود 101.8%
O=C(OC1CC(CO)C1O)c1ccccc1
2-Benzoyloxy-4-hydroxymethylcyclobutanol
المردود 101.8%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe ice bath removed
  2. 2
    workup.STIRRINGAfter stirring the reaction mixture for 35 minutes
  3. 3
    أخرىthe reaction was quenched with ~2 mL of methanol
  4. 4
    تركيزthe reaction mixture was concentrated in vacuo to a syrup
  5. 5
    workup.DISSOLUTIONThe syrup was dissolved in 250 mL of ethyl acetate
  6. 6
    غسيلthe ethyl acetate solution was washed with water and 5% aqueous sodium bicarbonate
  7. 7
    تجفيفdried over magnesium sulfate
  8. 8
    ترشيحfiltered
  9. 9
    تركيزconcentrated

الإجراء التجريبي

Glacial acetic acid in (25 mL) a 250 mL 3-neck flask was cooled in an ice bath under a stream of nitrogen. Sodium borohydride was added cautiously in portions over a 5 minute period. The ice bath removed and the reagent was used after stirring for 15 minutes at ambient temperature. 2-Benzoyloxy-4-hydroxymethylcyclobutanone (1.43 g, 6.5 mmol) from Step H was dissolved in 45 mL of glacial actetic acid and immediately treated with the above borohydride reagent. After stirring the reaction mixture for 35 minutes, the reaction was quenched with ~2 mL of methanol and the reaction mixture was concentrated in vacuo to a syrup. The syrup was dissolved in 250 mL of ethyl acetate and the ethyl acetate solution was washed with water and 5% aqueous sodium bicarbonate, dried over magnesium sulfate, filtered and concentrated to give 1.47 g of the title compound which was taken on to the next step without purification; MS DCI-NH3M/Z: 221 (M+H)+, 238 (M+NH4)+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05246931uspto-grants-1993_09