돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 67798생성일: 2026년 10월 23일

Pivalic acid → 4-Methoxycarbonylmethyl-4-(3'-methoxyphenyl)-1-methyl-3-methylene-2-piperidone

https://huagongshe.com/ko/reaction/67798

반응식

참여 물질

역할이름HCID투입량
반응물Pivalic acidHCID 6417—
반응물Trimethyl orthoacetateHCID 15050—
반응물3-Hydroxymethyl-4-(3'-methoxyphenyl)-1-methyl-5,6-dihydro-2-pyridoneHCID 13107980—
용매DiglymeHCID 8150—
생성물4-Methoxycarbonylmethyl-4-(3'-methoxyphenyl)-1-methyl-3-methylene-2-piperidoneHCID 12947553—

반응 단계

The allylic alcohol 27 of Example 9 (1.22 g, 4.96 mmol), trimethyl orthoacetate (5.52 g, 46 mmol), and pivalic acid (25 mg, 0.50 mmol) were placed in diglyme (25 mL) and refluxed at 155°-160° C. (internal) with fractionation to remove CH3OH. after 18 h the solvents were evaporated and the residue distilled [bp 175°-185° C. (0.15 mm)] to return 1.21 g (80%) of methyl ester 28. Upon standing the ester crystallized: mp 85°-86° C.; NMR δ7.30 (m, 1H), 6.86 (m, 4H), 6.65 (s, 1H), 5.57 (s, 1H), 3.76 (s, 3H), 3.47 (s 3H), 3.17 (m, 3H), 2.87 (s, 4H), 2.53 (m, 2H); IR 1733, 1653, 1595 cm-1 ; mass spectrum m/e (rel intensity) 303 (38), 230 (100). Anal. Calcd for C17H21NO4 : C, 67.3; H, 7.0; N, 4.6. Found: C, 67.2; H, 7.0; N, 4.6.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04346224
출처 데이터셋uspto-grants-1982_08
ORD IDord-1c22feec8e68477d9dec17d225a43063
출처 메모uspto-grants-1982_08