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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 2-(Pyrrolidin-1-yl)acetic acid hydrochloride

HRID 370334
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HRID 370334 반응식
Br[CH2:2][C:3]([O:5]C(C)(C)C)=[O:4].[NH:10]1[CH2:14][CH2:13][CH2:12][CH2:11]1.[ClH:15]>C1COCC1.O1CCOCC1>[ClH:15].[N:10]1([CH2:2][C:3]([OH:5])=[O:4])[CH2:14][CH2:13][CH2:12][CH2:11]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 31268PyrrolidineHCID 79177tert-Butyl bromoacetate

생성물 1

HCID 130220162-(Pyrrolidin-1-yl)acetic acid hydrochloride수율 97.4%

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매2회HCID 312751,4-Dioxane용매

실험 절차

A solution of 19.6 g (101 mmol) of t-butyl bromoacetate in 150 mL of THF was cooled in an ice bath and treated dropwise over about 0.5 hour with a solution of 14.4 g (202 mmol) of pyrrolidine in 75 mL of THF, to produce a white precipitate. The bath was removed and the reaction slurry stirred for two hours. The solid was removed by filtration and the filtrate was concentrated under reduced pressure to yield a clear liquid over an orange-colored solid. The liquid was cooled in an ice bath, then treated with 40 mL (80 mmol) of 4N HCl in dioxane and stirred for 15 hours. The solvents were removed in vacuo, and the residue was triturated with diethyl ether, then filtered to yield 12.9 g of the desired acid as an off-white solid.

후처리

  1. customto produce a white precipitate
  2. customThe bath was removed
  3. customThe solid was removed by filtration
  4. concentrationthe filtrate was concentrated under reduced pressure
  5. customto yield a clear liquid over an orange-colored solid
  6. temperatureThe liquid was cooled in an ice bath
  7. stirringstirred for 15 hours
  8. customThe solvents were removed in vacuo
  9. customthe residue was triturated with diethyl ether
  10. filtrationfiltered

출처 및 근거

ORD 기록
ord-9cced26fcdcd40c7be9706007486f4b4
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06140505

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