Hydrochloric Acid → (S)-(+)-3-Cyano-4-(2-methylbutyloxy)phenylboronic acid

HRID 442586노트

반응식

HRID 442586 반응식
[Li].[C:2]([C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][C:12]=1[O:13][CH2:14][C@@H:15]([CH3:18])[CH2:16][CH3:17])C(O)=O)#[N:3].[B:19](OC)([O:22]C)[O:20]C.Cl>C1COCC1>[C:2]([C:4]1[CH:5]=[C:6]([B:19]([OH:22])[OH:20])[CH:10]=[CH:11][C:12]=1[O:13][CH2:14][C@@H:15]([CH3:18])[CH2:16][CH3:17])#[N:3]

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 8470Trimethyl borateHCID 3028194Lithium2회HCID 54501986(S)-(+)-3-Cyano-4-(2-methylbutyloxy)benzoic acid

생성물 1

HCID 53923893(S)-(+)-3-Cyano-4-(2-methylbutyloxy)phenylboronic acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

The experimental procedure for the preparation of the lithium salt was as described in the preparation of compound 43. A solution of trimethyl borate (2.70 g, 0.024 mol) in dry THF (10 ml) was added dropwise to the lithium salt solution. The resultant mixture was allowed to warm to room temperature overnight whilst stirring and dilute hydrochloric acid was then added. The THF/water azeotrope was removed in vacuo and the remaining residue was dissolved in diethyl ether and washed with water until acid-free. The ether was dried (MgSO4) and removed in vacuo to leave a fawn solid.

후처리

  1. customThe THF/water azeotrope was removed in vacuo
  2. dissolutionthe remaining residue was dissolved in diethyl ether
  3. washwashed with water until acid-free
  4. dry with materialThe ether was dried (MgSO4)
  5. customremoved in vacuo
  6. customto leave a fawn solid

출처 및 근거

ORD 기록
ord-8d36b30d02454af9b5c685ec55fb20d7
출처 데이터셋
uspto-grants-1999_04
특허 번호
US05891358

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