تفاعل #5637
ord-f09896308b314dc9afd1bacf46b0ac34
معادلة التفاعل
ethyl chloroformate
product
(+/-)-2'-(2-Aminoethyl)-3',4'-dihydrospiro[cyclopentane-1,1'(2'H)-napthalen]-2'-ol
triethylamine
→
title compound
المردود 98.0%
Ethyl (+/-)-[2-(3',4'-dihydro-2'-hydroxyspiro[cyclopentane-1,1'(2'H)-napthalen]-2'-yl)ethyl]carbamate
المردود 98.0%
المتفاعلات
الكواشف
لا شيء
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1غسيلwashed with water
- 2استخلاصThe aqueous phase was extracted with CH2Cl2 (3×20 mL)
- 3تجفيفthe combined organic extracts were dried (MgSO4)
- 4ترشيحfiltered
- 5تركيزconcentrated
- 6أخرىThe residue was purified by chromatography (silica gel, 1:1 heptane/ethyl acetate)
الإجراء التجريبي
A solution of the product from Example 9 (1.05 g, 4.28 mmol) and triethylamine (0.44 g, 4.35 mmol) in 10 mL of CH2Cl2 was cooled to 0° C. and ethyl chloroformate (0.47 g, 4.33 mmol) in 5 mL CH2Cl2 was added dropwise. The reaction was warmed to room temperature and washed with water. The aqueous phase was extracted with CH2Cl2 (3×20 mL) and the combined organic extracts were dried (MgSO4), filtered and concentrated. The residue was purified by chromatography (silica gel, 1:1 heptane/ethyl acetate) to give the title compound (1.33 g, 98%) as an oil.