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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Formaldehyde → (N-benzylglycylmethyl)hydroxymethylphosphinic acid

HRID 224522
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반응식

HRID 224522 반응식
[OH:1][CH2:2][P:3]([OH:5])[OH:4].Cl.[CH2:7]([NH:14][CH2:15][C:16]([OH:18])=O)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[CH2:19]=O>Cl>[CH2:7]([NH:14][CH2:15][C:16]([CH2:19][P:3]([CH2:2][OH:1])(=[O:5])[OH:4])=[O:18])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 712FormaldehydeHCID 2756624N-Benzylglycine HydrochlorideHCID 23330988Hydroxymethylphosphonous acid

생성물 1

HCID 54414086(N-benzylglycylmethyl)hydroxymethylphosphinic acid수율 88%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

The procedure of Example 1 is carried out starting from 9.6 g (0.1 mole) of hydroxymethylphosphonous acid ##STR8## 20.2 g (0.1 mole) of N-benzylglycine hydrochloride, 100 ml of conc. hydrochloric acid and 31.6 g of 38% formaldehyde solution. The reaction mixture is concentrated by rotary evaporation, yielding 22.7 g (88%) of (N-benzylglycylmethyl)hydroxymethylphosphinic acid of the formula ##STR9## as a glassy substance which sinters at 92° C., becomes liquid at 118° C., and decomposes at 135° C.

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후처리

  1. concentrationThe reaction mixture is concentrated by rotary evaporation

출처 및 근거

ORD 기록
ord-26e3264fcbf5468f95067205d987fe19
출처 데이터셋
uspto-grants-1980_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04233056

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