تفاعل #363431

ord-96e8f18f2acb48c4a45d10eda0248a35

معادلة التفاعل

NC1(C(=O)O)CCCCC1
l-aminocyclohexane-1-carboxylic acid
O=C(Cl)OCc1ccccc1
benzyl chloroformate
O=C(NC1(C(=O)O)CCCCC1)OCc1ccccc1
1-(benzyloxycarbonylamino)cyclohexane-1-carboxylic acid
المردود 89.1%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwhile maintaining pH 9
  2. 2
    غسيلThe resulting solution was washed with Et2O (2×100 mL)
  3. 3
    استخلاصthe solution was extracted with EtOAc (3×150 mL)
  4. 4
    تجفيفThe combined organic layers were dried (MgSO4)
  5. 5
    تركيزconcentrated under reduced pressure

الإجراء التجريبي

To a solution of l-aminocyclohexane-1-carboxylic acid (10.0 g, 70.0 mmol) in a 1M NaOH solution (100 mL) was added benzyl chloroformate (12.0 ml, 84.0 mmol). The reaction mixture was stirred for 2 h while maintaining pH 9 by addition of a 1M NaOH solution as necessary. The resulting solution was washed with Et2O (2×100 mL), then the aqueous layer was adjusted to pH 0 with a conc. HCl solution and the solution was extracted with EtOAc (3×150 mL). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure to yield 1-(benzyloxycarbonylamino)cyclohexane-1-carboxylic acid (17.3 g, 89%): TLC (25% EtOAc/hex) Rf0.07.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06353006B1uspto-grants-2002_03